Canonical Allele Identifier: CA2715918330
Gene: ATP6V0A4 HGNC NCBI

Linked Data

dbSNP Id: rs2117166097

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138706500T>C , CM000669.2:g.138706500T>C GRCh38
NC_000007.13:g.138391245T>C , CM000669.1:g.138391245T>C GRCh37
NC_000007.12:g.138041785T>C NCBI36
NG_008145.1:g.96697A>G
NG_051552.1:g.48A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000310018.7:c.*124A>G MANE Select ENSP00000308122.2:n.*124A>G
ENST00000478480.2:c.*212A>G ENSP00000495261.1:n.*212A>G
ENST00000644341.1:c.*124A>G ENSP00000495642.1:n.*124A>G
ENST00000645515.1:c.*124A>G ENSP00000496421.1:n.*124A>G
ENST00000647427.1:c.1422A>G ENSP00000496259.1:n.1422A>G
ENST00000310018.6:c.*124A>G ENSP00000308122.2:n.*124A>G
ENST00000393054.5:c.*124A>G ENSP00000376774.1:n.*124A>G
NM_020632.2:c.*124A>G NP_065683.2:n.*124A>G
NM_130840.2:c.*124A>G NP_570855.2:n.*124A>G
NM_130841.2:c.*124A>G NP_570856.2:n.*124A>G
XM_005250393.1:c.*124A>G XP_005250450.1:n.*124A>G
XM_005250394.2:c.*124A>G XP_005250451.1:n.*124A>G
XM_005250394.3:c.*124A>G XP_005250451.1:n.*124A>G
NM_020632.3:c.*124A>G MANE Select NP_065683.2:n.*124A>G
NM_130840.3:c.*124A>G NP_570855.2:n.*124A>G
NM_130841.3:c.*124A>G NP_570856.2:n.*124A>G