Canonical Allele Identifier: CA2069005163

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744558T= , CM000674.2:g.123744558T=	GRCh38
NC_000012.11:g.124229105T= , CM000674.1:g.124229105T=	GRCh37
NC_000012.10:g.122795058T=	NCBI36
NG_012743.1:g.37241T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1327-39T= MANE Select	ENSP00000332247.2:n.1327-39T=
ENST00000540368.6:n.1358-39T=
ENST00000674794.1:c.1415-39T=
ENST00000675260.1:n.602-39T=
ENST00000675344.1:c.*348-39T=	ENSP00000501953.1:n.*348-39T=
ENST00000330342.7:c.1327-39T=	ENSP00000332247.2:n.1327-39T=
ENST00000504192.2:c.937-39T=	ENSP00000443441.1:n.937-39T=
ENST00000536426.1:n.344-39T=
ENST00000545059.5:n.3963-39T=
NM_012463.3:c.1327-39T=	NP_036595.2:n.1327-39T=
XM_005253563.1:c.1327-39T=	XP_005253620.1:n.1327-39T=
XM_006719317.2:c.814-39T=	XP_006719380.1:n.814-39T=
XM_006719318.2:c.505-39T=	XP_006719381.1:n.505-39T=
XR_429088.1:n.1490-39T=
XM_024448910.1:c.1327-39T=	XP_024304678.1:n.1327-39T=
XM_024448911.1:c.814-39T=	XP_024304679.1:n.814-39T=
XM_024448912.1:c.505-39T=	XP_024304680.1:n.505-39T=
NM_012463.4:c.1327-39T= MANE Select	NP_036595.2:n.1327-39T=