Canonical Allele Identifier: CA2068978827

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123726279A= , CM000674.2:g.123726279A=	GRCh38
NC_000012.11:g.124210826A= , CM000674.1:g.124210826A=	GRCh37
NC_000012.10:g.122776779A=	NCBI36
NG_012743.1:g.18962A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330342.8:c.515A= MANE Select	ENSP00000332247.2:p.Lys172=
ENST00000540368.6:n.546A=
ENST00000613625.5:c.515A=	ENSP00000482236.1:p.Lys172=
ENST00000675344.1:c.515A=	ENSP00000501953.1:p.Lys172=
ENST00000330342.7:c.515A=	ENSP00000332247.2:p.Lys172=
ENST00000504192.2:c.125A=	ENSP00000443441.1:p.Lys42=
ENST00000540368.5:n.725A=
ENST00000613625.4:c.515A=	ENSP00000482236.1:p.Lys172=
NM_012463.3:c.515A=	NP_036595.2:p.Lys172=
XM_005253563.1:c.515A=	XP_005253620.1:p.Lys172=
XM_006719317.2:c.8+1488A=	XP_006719380.1:n.8+1488A=
XR_429088.1:n.678A=
XM_024448910.1:c.515A=	XP_024304678.1:p.Lys172=
XM_024448911.1:c.8+1488A=	XP_024304679.1:n.8+1488A=
NM_012463.4:c.515A= MANE Select	NP_036595.2:p.Lys172=