Canonical Allele Identifier: CA1746763209

Gene: ATP6V0A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138706668G= , CM000669.2:g.138706668G=	GRCh38
NC_000007.13:g.138391413G= , CM000669.1:g.138391413G=	GRCh37
NC_000007.12:g.138041953G=	NCBI36
NG_008145.1:g.96529C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310018.7:c.2479C= MANE Select	ENSP00000308122.2:p.Pro827=
ENST00000478480.2:c.*44C=	ENSP00000495261.1:n.*44C=
ENST00000644341.1:c.1705C=	ENSP00000495642.1:p.Pro569=
ENST00000645515.1:c.2479C=	ENSP00000496421.1:p.Pro827=
ENST00000647427.1:c.1254C=	ENSP00000496259.1:n.1254C=
ENST00000310018.6:c.2479C=	ENSP00000308122.2:p.Pro827=
ENST00000353492.4:c.2479C=	ENSP00000253856.6:p.Pro827=
ENST00000393054.5:c.2479C=	ENSP00000376774.1:p.Pro827=
NM_020632.2:c.2479C=	NP_065683.2:p.Pro827=
NM_130840.2:c.2479C=	NP_570855.2:p.Pro827=
NM_130841.2:c.2479C=	NP_570856.2:p.Pro827=
XM_005250393.1:c.2479C=	XP_005250450.1:p.Pro827=
XM_005250394.2:c.2479C=	XP_005250451.1:p.Pro827=
XM_005250394.3:c.2479C=	XP_005250451.1:p.Pro827=
NM_020632.3:c.2479C= MANE Select	NP_065683.2:p.Pro827=
NM_130840.3:c.2479C=	NP_570855.2:p.Pro827=
NM_130841.3:c.2479C=	NP_570856.2:p.Pro827=