Canonical Allele Identifier: CA2069003783

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123743852G= , CM000674.2:g.123743852G=	GRCh38
NC_000012.11:g.124228399G= , CM000674.1:g.124228399G=	GRCh37
NC_000012.10:g.122794352G=	NCBI36
NG_012743.1:g.36535G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1106G= MANE Select	ENSP00000332247.2:p.Arg369=
ENST00000540368.6:n.1137G=
ENST00000674794.1:c.1194G=
ENST00000675260.1:n.381G=
ENST00000675344.1:c.*127G=	ENSP00000501953.1:n.*127G=
ENST00000330342.7:c.1106G=	ENSP00000332247.2:p.Arg369=
ENST00000504192.2:c.716G=	ENSP00000443441.1:p.Arg239=
ENST00000536426.1:n.123G=
ENST00000545059.5:n.3742G=
NM_012463.3:c.1106G=	NP_036595.2:p.Arg369=
XM_005253563.1:c.1106G=	XP_005253620.1:p.Arg369=
XM_006719317.2:c.593G=	XP_006719380.1:p.Arg198=
XM_006719318.2:c.284G=	XP_006719381.1:p.Arg95=
XR_429088.1:n.1269G=
XM_024448910.1:c.1106G=	XP_024304678.1:p.Arg369=
XM_024448911.1:c.593G=	XP_024304679.1:p.Arg198=
XM_024448912.1:c.284G=	XP_024304680.1:p.Arg95=
NM_012463.4:c.1106G= MANE Select	NP_036595.2:p.Arg369=