Canonical Allele Identifier: CA2069004471

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744225C= , CM000674.2:g.123744225C=	GRCh38
NC_000012.11:g.124228772C= , CM000674.1:g.124228772C=	GRCh37
NC_000012.10:g.122794725C=	NCBI36
NG_012743.1:g.36908C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1214C= MANE Select	ENSP00000332247.2:p.Pro405=
ENST00000540368.6:n.1245C=
ENST00000674794.1:c.1302C=
ENST00000675260.1:n.489C=
ENST00000675344.1:c.*235C=	ENSP00000501953.1:n.*235C=
ENST00000330342.7:c.1214C=	ENSP00000332247.2:p.Pro405=
ENST00000504192.2:c.824C=	ENSP00000443441.1:p.Pro275=
ENST00000536426.1:n.231C=
ENST00000545059.5:n.3850C=
NM_012463.3:c.1214C=	NP_036595.2:p.Pro405=
XM_005253563.1:c.1214C=	XP_005253620.1:p.Pro405=
XM_006719317.2:c.701C=	XP_006719380.1:p.Pro234=
XM_006719318.2:c.392C=	XP_006719381.1:p.Pro131=
XR_429088.1:n.1377C=
XM_024448910.1:c.1214C=	XP_024304678.1:p.Pro405=
XM_024448911.1:c.701C=	XP_024304679.1:p.Pro234=
XM_024448912.1:c.392C=	XP_024304680.1:p.Pro131=
NM_012463.4:c.1214C= MANE Select	NP_036595.2:p.Pro405=