Canonical Allele Identifier: CA2068977443

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123724789G= , CM000674.2:g.123724789G=	GRCh38
NC_000012.11:g.124209336G= , CM000674.1:g.124209336G=	GRCh37
NC_000012.10:g.122775289G=	NCBI36
NG_012743.1:g.17472G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.430G= MANE Select	ENSP00000332247.2:p.Glu144=
ENST00000540368.6:n.461G=
ENST00000613625.5:c.430G=	ENSP00000482236.1:p.Glu144=
ENST00000675344.1:c.430G=	ENSP00000501953.1:p.Glu144=
ENST00000330342.7:c.430G=	ENSP00000332247.2:p.Glu144=
ENST00000504192.2:c.40G=	ENSP00000443441.1:p.Glu14=
ENST00000540368.5:n.640G=
ENST00000613625.4:c.430G=	ENSP00000482236.1:p.Glu144=
NM_012463.3:c.430G=	NP_036595.2:p.Glu144=
XM_005253563.1:c.430G=	XP_005253620.1:p.Glu144=
XM_006719317.2:c.6G=	XP_006719380.1:p.Leu2=
XR_429088.1:n.593G=
XM_024448910.1:c.430G=	XP_024304678.1:p.Glu144=
XM_024448911.1:c.6G=	XP_024304679.1:p.Leu2=
NM_012463.4:c.430G= MANE Select	NP_036595.2:p.Glu144=