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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
Genomic
-
NG_042093.1Â RefSeqGene
- Range
-
5040..127548
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001305878.2 → NP_001292807.1  histone acetyltransferase KAT6A isoform 2
See identical proteins and their annotated locations for NP_001292807.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) lacks several exons in the 3' coding region and its 3' terminal exon extends past a splice site that is used in variant 1, resulting in differences in the 3' coding region and 3' UTR compared to variant 1. It encodes isoform 2, which has a shorter and distinct C-terminus compared to isoform 1.
- Source sequence(s)
-
AC090571, BC142959, BP271264
- Consensus CDS
-
CCDS83290.1
- UniProtKB/TrEMBL
-
A5PLL3
- Related
- ENSP00000430606.1, ENST00000485568.5
- Conserved Domains (5) summary
-
- smart00526
Location:85 → 162
- H15; Domain in histone families 1 and 5
- cd15527
Location:264 → 310
- PHD2_KAT6A_6B; PHD finger 2 found in monocytic leukemia zinc-finger protein (MOZ) and its factor (MORF)
- cd15618
Location:205 → 262
- PHD1_MOZ_MORF; PHD finger 1 found in monocytic leukemia zinc-finger protein (MOZ) and its factor (MORF)
- pfam01853
Location:565 → 743
- MOZ_SAS; MOZ/SAS family
- cl17182
Location:505 → 779
- NAT_SF; N-Acyltransferase superfamily: Various enyzmes that characteristicly catalyze the transfer of an acyl group to a substrate
-
NM_006766.5 → NP_006757.2  histone acetyltransferase KAT6A isoform 1
See identical proteins and their annotated locations for NP_006757.2
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1).
- Source sequence(s)
-
AA310750, AC090571, AJ420560, BC142659, CB216817, DA442995, U47742
- Consensus CDS
-
CCDS6124.1
- UniProtKB/Swiss-Prot
-
Q92794
- UniProtKB/TrEMBL
-
A0A3F2YNX6
- Related
- ENSP00000265713.2, ENST00000265713.8
- Conserved Domains (4) summary
-
- smart00526
Location:85 → 162
- H15; Domain in histone families 1 and 5
- PLN00104
Location:504 → 778
- PLN00104; MYST -like histone acetyltransferase; Provisional
- cd15527
Location:264 → 310
- PHD2_KAT6A_6B; PHD finger 2 found in monocytic leukemia zinc-finger protein (MOZ) and its factor (MORF)
- cd15618
Location:205 → 262
- PHD1_MOZ_MORF; PHD finger 1 found in monocytic leukemia zinc-finger protein (MOZ) and its factor (MORF)
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000008.11Â Reference GRCh38.p14 Primary Assembly
- Range
-
41929479..42051987 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060932.1Â Alternate T2T-CHM13v2.0
- Range
-
42203787..42326296 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the
cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related
sequence links, or BLAST links (BLink), but may still be retrieved by clicking on
their accession.version below.
-
NM_001099412.1: Suppressed sequence
- Description
- NM_001099412.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript.
-
NM_001099413.1: Suppressed sequence
- Description
- NM_001099413.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript.