Canonical Allele Identifier: CA1746779957
Gene: ATP6V0A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138739387G= , CM000669.2:g.138739387G= GRCh38
NC_000007.13:g.138424132G= , CM000669.1:g.138424132G= GRCh37
NC_000007.12:g.138074672G= NCBI36
NG_008145.1:g.63810C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310018.7:c.1572+153C= MANE Select ENSP00000308122.2:n.1572+153C=
ENST00000478480.2:c.798+153C= ENSP00000495261.1:n.798+153C=
ENST00000644341.1:c.798+153C= ENSP00000495642.1:n.798+153C=
ENST00000645515.1:c.1572+153C= ENSP00000496421.1:n.1572+153C=
ENST00000647427.1:c.465+153C= ENSP00000496259.1:n.465+153C=
ENST00000310018.6:c.1572+153C= ENSP00000308122.2:n.1572+153C=
ENST00000353492.4:c.1572+153C= ENSP00000253856.6:n.1572+153C=
ENST00000393054.5:c.1572+153C= ENSP00000376774.1:n.1572+153C=
ENST00000471085.1:n.252-5133C=
NM_020632.2:c.1572+153C= NP_065683.2:n.1572+153C=
NM_130840.2:c.1572+153C= NP_570855.2:n.1572+153C=
NM_130841.2:c.1572+153C= NP_570856.2:n.1572+153C=
XM_005250393.1:c.1572+153C= XP_005250450.1:n.1572+153C=
XM_005250394.2:c.1572+153C= XP_005250451.1:n.1572+153C=
XM_005250394.3:c.1572+153C= XP_005250451.1:n.1572+153C=
NM_020632.3:c.1572+153C= MANE Select NP_065683.2:n.1572+153C=
NM_130840.3:c.1572+153C= NP_570855.2:n.1572+153C=
NM_130841.3:c.1572+153C= NP_570856.2:n.1572+153C=