Canonical Allele Identifier: CA2068991990

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123737085G= , CM000674.2:g.123737085G=	GRCh38
NC_000012.11:g.124221632G= , CM000674.1:g.124221632G=	GRCh37
NC_000012.10:g.122787585G=	NCBI36
NG_012743.1:g.29768G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330342.8:c.852G= MANE Select	ENSP00000332247.2:p.Leu284=
ENST00000540368.6:n.883G=
ENST00000613625.5:c.852G=	ENSP00000482236.1:p.Leu284=
ENST00000674794.1:c.940G=
ENST00000675344.1:c.852G=	ENSP00000501953.1:p.Leu284=
ENST00000330342.7:c.852G=	ENSP00000332247.2:p.Leu284=
ENST00000504192.2:c.462G=	ENSP00000443441.1:p.Leu154=
ENST00000540368.5:n.1062G=
ENST00000545059.5:n.3488G=
ENST00000613625.4:c.852G=	ENSP00000482236.1:p.Leu284=
NM_012463.3:c.852G=	NP_036595.2:p.Leu284=
XM_005253563.1:c.852G=	XP_005253620.1:p.Leu284=
XM_006719317.2:c.339G=	XP_006719380.1:p.Leu113=
XM_006719318.2:c.30G=	XP_006719381.1:p.Leu10=
XR_429088.1:n.1015G=
XM_024448910.1:c.852G=	XP_024304678.1:p.Leu284=
XM_024448911.1:c.339G=	XP_024304679.1:p.Leu113=
XM_024448912.1:c.30G=	XP_024304680.1:p.Leu10=
NM_012463.4:c.852G= MANE Select	NP_036595.2:p.Leu284=