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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_001320218.2 → NP_001307147.1 V-type proton ATPase subunit G 3 isoform c
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) encodes the longest isoform (c).
- Source sequence(s)
-
BC101129, BF509031, BX114684
- Consensus CDS
-
CCDS81414.1
- UniProtKB/Swiss-Prot
-
Q96LB4
- Conserved Domains (1) summary
-
- pfam03179
Location:3 → 113
- V-ATPase_G; Vacuolar (H+)-ATPase G subunit
-
NM_001376861.1 → NP_001363790.1 V-type proton ATPase subunit G 3 isoform a
Status: REVIEWED
- Source sequence(s)
-
AI791754, BC101130, BF509031
- Consensus CDS
-
CCDS1395.1
- UniProtKB/Swiss-Prot
- Q495K2, Q495K4, Q5T9L6, Q96LB4
- Related
- ENSP00000356352.2, ENST00000367382.6
- Conserved Domains (1) summary
-
- pfam03179
Location:3 → 107
- V-ATPase_G; Vacuolar (H+)-ATPase G subunit
-
NM_001376862.1 → NP_001363791.1 V-type proton ATPase subunit G 3 isoform c
Status: REVIEWED
- Source sequence(s)
-
AI791754, BC101129, BF509031
- Consensus CDS
-
CCDS81414.1
- Related
- ENSP00000417171.1, ENST00000489986.1
- Conserved Domains (1) summary
-
- pfam03179
Location:3 → 113
- V-ATPase_G; Vacuolar (H+)-ATPase G subunit
-
NM_001376863.1 → NP_001363792.1 V-type proton ATPase subunit G 3 isoform b
Status: REVIEWED
- Source sequence(s)
-
AI791754, BC101131, BF509031
- Consensus CDS
-
CCDS1396.1
- Conserved Domains (1) summary
-
- cl03922
Location:3 → 27
- V-ATPase_G; Vacuolar (H+)-ATPase G subunit
-
NM_133262.3 → NP_573569.1 V-type proton ATPase subunit G 3 isoform a
See identical proteins and their annotated locations for NP_573569.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) lacks an alternate in-frame exon in the 5' coding region, compared to variant 3. It encodes isoform a, which lacks an internal segment and is shorter, compared to isoform c.
- Source sequence(s)
-
BC101130, BF509031, BX114684
- Consensus CDS
-
CCDS1395.1
- UniProtKB/Swiss-Prot
- Q495K2, Q495K4, Q5T9L6, Q96LB4
- Related
- ENSP00000281087.2, ENST00000281087.6
- Conserved Domains (1) summary
-
- pfam03179
Location:3 → 107
- V-ATPase_G; Vacuolar (H+)-ATPase G subunit
-
NM_133326.2 → NP_579872.1 V-type proton ATPase subunit G 3 isoform b
See identical proteins and their annotated locations for NP_579872.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) uses an alternate splice site in the 5' coding region, compared to variant 3, resulting in a frameshift and an early stop codon. It encodes isoform b, which is shorter and has a distinct C-terminus, compared to isoform c.
- Source sequence(s)
-
BF509031
- Consensus CDS
-
CCDS1396.1
- UniProtKB/Swiss-Prot
-
Q96LB4
- Related
- ENSP00000309574.7, ENST00000309309.11
- Conserved Domains (1) summary
-
- cl03922
Location:3 → 27
- V-ATPase_G; Vacuolar (H+)-ATPase G subunit
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_000001.11 Reference GRCh38.p14 Primary Assembly
- Range
-
198523222..198540945 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Reference GRCh38.p14 ALT_REF_LOCI_1
Genomic
-
NW_003315907.2 Reference GRCh38.p14 ALT_REF_LOCI_1
- Range
-
164628..182350 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060925.1 Alternate T2T-CHM13v2.0
- Range
-
197783117..197800839 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)