Canonical Allele Identifier: CA2068977460

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123724803C= , CM000674.2:g.123724803C=	GRCh38
NC_000012.11:g.124209350C= , CM000674.1:g.124209350C=	GRCh37
NC_000012.10:g.122775303C=	NCBI36
NG_012743.1:g.17486C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.432+12C= MANE Select	ENSP00000332247.2:n.432+12C=
ENST00000540368.6:n.463+12C=
ENST00000613625.5:c.432+12C=	ENSP00000482236.1:n.432+12C=
ENST00000675344.1:c.432+12C=	ENSP00000501953.1:n.432+12C=
ENST00000330342.7:c.432+12C=	ENSP00000332247.2:n.432+12C=
ENST00000504192.2:c.42+12C=	ENSP00000443441.1:n.42+12C=
ENST00000540368.5:n.642+12C=
ENST00000613625.4:c.432+12C=	ENSP00000482236.1:n.432+12C=
NM_012463.3:c.432+12C=	NP_036595.2:n.432+12C=
XM_005253563.1:c.432+12C=	XP_005253620.1:n.432+12C=
XM_006719317.2:c.8+12C=	XP_006719380.1:n.8+12C=
XR_429088.1:n.595+12C=
XM_024448910.1:c.432+12C=	XP_024304678.1:n.432+12C=
XM_024448911.1:c.8+12C=	XP_024304679.1:n.8+12C=
NM_012463.4:c.432+12C= MANE Select	NP_036595.2:n.432+12C=