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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.
mRNA and Protein(s)
-
NM_001303120.1 → NP_001290049.1 keratin-associated protein 19-6 isoform KRTAP19-6-V2
See identical proteins and their annotated locations for NP_001290049.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (KRTAP19-6-V2), which is produced by a polymorphic allele found in the alternate CHM1_1.1 and HuRef genome assemblies, differs at a single nucleotide position (reference SNP rs1023364) and contains a 1-nucleotide deletion (reference SNP rs5843453), resulting in a longer 3' coding region, compared to variant KRTAP19-6-V1. The encoded isoform (KRTAP19-6-V2) has a distinct and longer C-terminus, compared to isoform KRTAP19-6-V1.
- Source sequence(s)
-
AB096948, BC101815
- UniProtKB/TrEMBL
-
A4FU57
-
NM_181612.3 → NP_853643.1 keratin-associated protein 19-6 isoform KRTAP19-6-V1
See identical proteins and their annotated locations for NP_853643.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (KRTAP19-6-V1), which is produced by the primary reference genome allele, represents the longer transcript and encodes the shorter isoform (KRTAP19-6-V1).
- Source sequence(s)
-
AB096947, AP000567, BC101813
- Consensus CDS
-
CCDS13598.1
- UniProtKB/Swiss-Prot
- Q3LI70, Q3LI71
- Related
- ENSP00000375107.3, ENST00000334046.5
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_000021.9 Reference GRCh38.p14 Primary Assembly
- Range
-
30541535..30541864 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060945.1 Alternate T2T-CHM13v2.0
- Range
-
28907495..28907823 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)