Canonical Allele Identifier: CA2069003987

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123743935G= , CM000674.2:g.123743935G=	GRCh38
NC_000012.11:g.124228482G= , CM000674.1:g.124228482G=	GRCh37
NC_000012.10:g.122794435G=	NCBI36
NG_012743.1:g.36618G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1189G= MANE Select	ENSP00000332247.2:p.Ala397=
ENST00000540368.6:n.1220G=
ENST00000674794.1:c.1277G=
ENST00000675260.1:n.464G=
ENST00000675344.1:c.*210G=	ENSP00000501953.1:n.*210G=
ENST00000330342.7:c.1189G=	ENSP00000332247.2:p.Ala397=
ENST00000504192.2:c.799G=	ENSP00000443441.1:p.Ala267=
ENST00000536426.1:n.206G=
ENST00000545059.5:n.3825G=
NM_012463.3:c.1189G=	NP_036595.2:p.Ala397=
XM_005253563.1:c.1189G=	XP_005253620.1:p.Ala397=
XM_006719317.2:c.676G=	XP_006719380.1:p.Ala226=
XM_006719318.2:c.367G=	XP_006719381.1:p.Ala123=
XR_429088.1:n.1352G=
XM_024448910.1:c.1189G=	XP_024304678.1:p.Ala397=
XM_024448911.1:c.676G=	XP_024304679.1:p.Ala226=
XM_024448912.1:c.367G=	XP_024304680.1:p.Ala123=
NM_012463.4:c.1189G= MANE Select	NP_036595.2:p.Ala397=