Canonical Allele Identifier: CA1107808041
Gene: ATP6V0A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138733239_138733240insCCCCAAAA , CM000669.2:g.138733239_138733240insCCCCAAAA GRCh38
NC_000007.13:g.138417984_138417985insCCCCAAAA , CM000669.1:g.138417984_138417985insCCCCAAAA GRCh37
NC_000007.12:g.138068524_138068525insCCCCAAAA NCBI36
NG_008145.1:g.69957_69958insTTTTGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000310018.7:c.1692-147_1692-146insTTTTGGGG MANE Select ENSP00000308122.2:n.1692-147_1692-146insTTTTGGGG
ENST00000478480.2:c.918-147_918-146insTTTTGGGG ENSP00000495261.1:n.918-147_918-146insTTTTGGGG
ENST00000644341.1:c.918-147_918-146insTTTTGGGG ENSP00000495642.1:n.918-147_918-146insTTTTGGGG
ENST00000645515.1:c.1692-147_1692-146insTTTTGGGG ENSP00000496421.1:n.1692-147_1692-146insTTTTGGGG
ENST00000647427.1:c.585-147_585-146insTTTTGGGG ENSP00000496259.1:n.585-147_585-146insTTTTGGGG
ENST00000310018.6:c.1692-147_1692-146insTTTTGGGG ENSP00000308122.2:n.1692-147_1692-146insTTTTGGGG
ENST00000353492.4:c.1692-147_1692-146insTTTTGGGG ENSP00000253856.6:n.1692-147_1692-146insTTTTGGGG
ENST00000393054.5:c.1692-147_1692-146insTTTTGGGG ENSP00000376774.1:n.1692-147_1692-146insTTTTGGGG
NM_020632.2:c.1692-147_1692-146insTTTTGGGG NP_065683.2:n.1692-147_1692-146insTTTTGGGG
NM_130840.2:c.1692-147_1692-146insTTTTGGGG NP_570855.2:n.1692-147_1692-146insTTTTGGGG
NM_130841.2:c.1692-147_1692-146insTTTTGGGG NP_570856.2:n.1692-147_1692-146insTTTTGGGG
XM_005250393.1:c.1692-147_1692-146insTTTTGGGG XP_005250450.1:n.1692-147_1692-146insTTTTGGGG
XM_005250394.2:c.1692-147_1692-146insTTTTGGGG XP_005250451.1:n.1692-147_1692-146insTTTTGGGG
XM_005250394.3:c.1692-147_1692-146insTTTTGGGG XP_005250451.1:n.1692-147_1692-146insTTTTGGGG
NM_020632.3:c.1692-147_1692-146insTTTTGGGG MANE Select NP_065683.2:n.1692-147_1692-146insTTTTGGGG
NM_130840.3:c.1692-147_1692-146insTTTTGGGG NP_570855.2:n.1692-147_1692-146insTTTTGGGG
NM_130841.3:c.1692-147_1692-146insTTTTGGGG NP_570856.2:n.1692-147_1692-146insTTTTGGGG