Canonical Allele Identifier: CA2069004647

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744311C= , CM000674.2:g.123744311C=	GRCh38
NC_000012.11:g.124228858C= , CM000674.1:g.124228858C=	GRCh37
NC_000012.10:g.122794811C=	NCBI36
NG_012743.1:g.36994C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1300C= MANE Select	ENSP00000332247.2:p.His434=
ENST00000540368.6:n.1331C=
ENST00000674794.1:c.1388C=
ENST00000675260.1:n.575C=
ENST00000675344.1:c.*321C=	ENSP00000501953.1:n.*321C=
ENST00000330342.7:c.1300C=	ENSP00000332247.2:p.His434=
ENST00000504192.2:c.910C=	ENSP00000443441.1:p.His304=
ENST00000536426.1:n.317C=
ENST00000545059.5:n.3936C=
NM_012463.3:c.1300C=	NP_036595.2:p.His434=
XM_005253563.1:c.1300C=	XP_005253620.1:p.His434=
XM_006719317.2:c.787C=	XP_006719380.1:p.His263=
XM_006719318.2:c.478C=	XP_006719381.1:p.His160=
XR_429088.1:n.1463C=
XM_024448910.1:c.1300C=	XP_024304678.1:p.His434=
XM_024448911.1:c.787C=	XP_024304679.1:p.His263=
XM_024448912.1:c.478C=	XP_024304680.1:p.His160=
NM_012463.4:c.1300C= MANE Select	NP_036595.2:p.His434=