Canonical Allele Identifier: CA1746780032

Gene: ATP6V0A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138739576C= , CM000669.2:g.138739576C=	GRCh38
NC_000007.13:g.138424321C= , CM000669.1:g.138424321C=	GRCh37
NC_000007.12:g.138074861C=	NCBI36
NG_008145.1:g.63621G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310018.7:c.1536G= MANE Select	ENSP00000308122.2:p.Val512=
ENST00000478480.2:c.762G=	ENSP00000495261.1:p.Val254=
ENST00000644341.1:c.762G=	ENSP00000495642.1:p.Val254=
ENST00000645515.1:c.1536G=	ENSP00000496421.1:p.Val512=
ENST00000647427.1:c.429G=	ENSP00000496259.1:p.Val143=
ENST00000310018.6:c.1536G=	ENSP00000308122.2:p.Val512=
ENST00000353492.4:c.1536G=	ENSP00000253856.6:p.Val512=
ENST00000393054.5:c.1536G=	ENSP00000376774.1:p.Val512=
ENST00000471085.1:n.252-5322G=
NM_020632.2:c.1536G=	NP_065683.2:p.Val512=
NM_130840.2:c.1536G=	NP_570855.2:p.Val512=
NM_130841.2:c.1536G=	NP_570856.2:p.Val512=
XM_005250393.1:c.1536G=	XP_005250450.1:p.Val512=
XM_005250394.2:c.1536G=	XP_005250451.1:p.Val512=
XM_005250394.3:c.1536G=	XP_005250451.1:p.Val512=
NM_020632.3:c.1536G= MANE Select	NP_065683.2:p.Val512=
NM_130840.3:c.1536G=	NP_570855.2:p.Val512=
NM_130841.3:c.1536G=	NP_570856.2:p.Val512=