Canonical Allele Identifier: CA2068997679

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123751008C= , CM000674.2:g.123751008C=	GRCh38
NC_000012.11:g.124235555C= , CM000674.1:g.124235555C=	GRCh37
NC_000012.10:g.122801508C=	NCBI36
NG_012743.1:g.43691C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330342.8:c.1936-102C= MANE Select	ENSP00000332247.2:n.1936-102C=
ENST00000540368.6:n.1967-102C=
ENST00000674794.1:c.2024-102C=
ENST00000675260.1:n.1211-102C=
ENST00000675344.1:c.*957-102C=	ENSP00000501953.1:n.*957-102C=
ENST00000330342.7:c.1936-102C=	ENSP00000332247.2:n.1936-102C=
ENST00000534943.5:c.-327C=	ENSP00000443726.1:n.-327C=
NM_012463.3:c.1936-102C=	NP_036595.2:n.1936-102C=
XM_005253563.1:c.1936-1275C=	XP_005253620.1:n.1936-1275C=
XM_006719317.2:c.1423-102C=	XP_006719380.1:n.1423-102C=
XM_006719318.2:c.1114-102C=	XP_006719381.1:n.1114-102C=
XR_429088.1:n.2099-102C=
XM_024448910.1:c.1936-1275C=	XP_024304678.1:n.1936-1275C=
XM_024448911.1:c.1423-102C=	XP_024304679.1:n.1423-102C=
XM_024448912.1:c.1114-102C=	XP_024304680.1:n.1114-102C=
NM_012463.4:c.1936-102C= MANE Select	NP_036595.2:n.1936-102C=