Canonical Allele Identifier: CA1746776959
Gene: ATP6V0A4 HGNC NCBI

Linked Data

dbSNP Id: rs1805117334

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138733203_138733204insC , CM000669.2:g.138733203_138733204insC GRCh38
NC_000007.13:g.138417948_138417949insC , CM000669.1:g.138417948_138417949insC GRCh37
NC_000007.12:g.138068488_138068489insC NCBI36
NG_008145.1:g.69993_69994insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000310018.7:c.1692-111_1692-110insG MANE Select ENSP00000308122.2:n.1692-111_1692-110insG
ENST00000478480.2:c.918-111_918-110insG ENSP00000495261.1:n.918-111_918-110insG
ENST00000644341.1:c.918-111_918-110insG ENSP00000495642.1:n.918-111_918-110insG
ENST00000645515.1:c.1692-111_1692-110insG ENSP00000496421.1:n.1692-111_1692-110insG
ENST00000647427.1:c.585-111_585-110insG ENSP00000496259.1:n.585-111_585-110insG
ENST00000310018.6:c.1692-111_1692-110insG ENSP00000308122.2:n.1692-111_1692-110insG
ENST00000353492.4:c.1692-111_1692-110insG ENSP00000253856.6:n.1692-111_1692-110insG
ENST00000393054.5:c.1692-111_1692-110insG ENSP00000376774.1:n.1692-111_1692-110insG
NM_020632.2:c.1692-111_1692-110insG NP_065683.2:n.1692-111_1692-110insG
NM_130840.2:c.1692-111_1692-110insG NP_570855.2:n.1692-111_1692-110insG
NM_130841.2:c.1692-111_1692-110insG NP_570856.2:n.1692-111_1692-110insG
XM_005250393.1:c.1692-111_1692-110insG XP_005250450.1:n.1692-111_1692-110insG
XM_005250394.2:c.1692-111_1692-110insG XP_005250451.1:n.1692-111_1692-110insG
XM_005250394.3:c.1692-111_1692-110insG XP_005250451.1:n.1692-111_1692-110insG
NM_020632.3:c.1692-111_1692-110insG MANE Select NP_065683.2:n.1692-111_1692-110insG
NM_130840.3:c.1692-111_1692-110insG NP_570855.2:n.1692-111_1692-110insG
NM_130841.3:c.1692-111_1692-110insG NP_570856.2:n.1692-111_1692-110insG