Canonical Allele Identifier: CA2069004675

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744327A= , CM000674.2:g.123744327A=	GRCh38
NC_000012.11:g.124228874A= , CM000674.1:g.124228874A=	GRCh37
NC_000012.10:g.122794827A=	NCBI36
NG_012743.1:g.37010A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1316A= MANE Select	ENSP00000332247.2:p.Gln439=
ENST00000540368.6:n.1347A=
ENST00000674794.1:c.1404A=
ENST00000675260.1:n.591A=
ENST00000675344.1:c.*337A=	ENSP00000501953.1:n.*337A=
ENST00000330342.7:c.1316A=	ENSP00000332247.2:p.Gln439=
ENST00000504192.2:c.926A=	ENSP00000443441.1:p.Gln309=
ENST00000536426.1:n.333A=
ENST00000545059.5:n.3952A=
NM_012463.3:c.1316A=	NP_036595.2:p.Gln439=
XM_005253563.1:c.1316A=	XP_005253620.1:p.Gln439=
XM_006719317.2:c.803A=	XP_006719380.1:p.Gln268=
XM_006719318.2:c.494A=	XP_006719381.1:p.Gln165=
XR_429088.1:n.1479A=
XM_024448910.1:c.1316A=	XP_024304678.1:p.Gln439=
XM_024448911.1:c.803A=	XP_024304679.1:p.Gln268=
XM_024448912.1:c.494A=	XP_024304680.1:p.Gln165=
NM_012463.4:c.1316A= MANE Select	NP_036595.2:p.Gln439=