Canonical Allele Identifier: CA2068977412

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123724770C= , CM000674.2:g.123724770C=	GRCh38
NC_000012.11:g.124209317C= , CM000674.1:g.124209317C=	GRCh37
NC_000012.10:g.122775270C=	NCBI36
NG_012743.1:g.17453C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.411C= MANE Select	ENSP00000332247.2:p.Thr137=
ENST00000540368.6:n.442C=
ENST00000613625.5:c.411C=	ENSP00000482236.1:p.Thr137=
ENST00000675344.1:c.411C=	ENSP00000501953.1:p.Thr137=
ENST00000330342.7:c.411C=	ENSP00000332247.2:p.Thr137=
ENST00000504192.2:c.21C=	ENSP00000443441.1:p.Thr7=
ENST00000540368.5:n.621C=
ENST00000613625.4:c.411C=	ENSP00000482236.1:p.Thr137=
NM_012463.3:c.411C=	NP_036595.2:p.Thr137=
XM_005253563.1:c.411C=	XP_005253620.1:p.Thr137=
XM_006719317.2:c.-14C=	XP_006719380.1:n.-14C=
XR_429088.1:n.574C=
XM_024448910.1:c.411C=	XP_024304678.1:p.Thr137=
XM_024448911.1:c.-14C=	XP_024304679.1:n.-14C=
NM_012463.4:c.411C= MANE Select	NP_036595.2:p.Thr137=