Canonical Allele Identifier: CA2069004511

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744234T= , CM000674.2:g.123744234T=	GRCh38
NC_000012.11:g.124228781T= , CM000674.1:g.124228781T=	GRCh37
NC_000012.10:g.122794734T=	NCBI36
NG_012743.1:g.36917T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1223T= MANE Select	ENSP00000332247.2:p.Phe408=
ENST00000540368.6:n.1254T=
ENST00000674794.1:c.1311T=
ENST00000675260.1:n.498T=
ENST00000675344.1:c.*244T=	ENSP00000501953.1:n.*244T=
ENST00000330342.7:c.1223T=	ENSP00000332247.2:p.Phe408=
ENST00000504192.2:c.833T=	ENSP00000443441.1:p.Phe278=
ENST00000536426.1:n.240T=
ENST00000545059.5:n.3859T=
NM_012463.3:c.1223T=	NP_036595.2:p.Phe408=
XM_005253563.1:c.1223T=	XP_005253620.1:p.Phe408=
XM_006719317.2:c.710T=	XP_006719380.1:p.Phe237=
XM_006719318.2:c.401T=	XP_006719381.1:p.Phe134=
XR_429088.1:n.1386T=
XM_024448910.1:c.1223T=	XP_024304678.1:p.Phe408=
XM_024448911.1:c.710T=	XP_024304679.1:p.Phe237=
XM_024448912.1:c.401T=	XP_024304680.1:p.Phe134=
NM_012463.4:c.1223T= MANE Select	NP_036595.2:p.Phe408=