Canonical Allele Identifier: CA2069004533

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744242A= , CM000674.2:g.123744242A=	GRCh38
NC_000012.11:g.124228789A= , CM000674.1:g.124228789A=	GRCh37
NC_000012.10:g.122794742A=	NCBI36
NG_012743.1:g.36925A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330342.8:c.1231A= MANE Select	ENSP00000332247.2:p.Met411=
ENST00000540368.6:n.1262A=
ENST00000674794.1:c.1319A=
ENST00000675260.1:n.506A=
ENST00000675344.1:c.*252A=	ENSP00000501953.1:n.*252A=
ENST00000330342.7:c.1231A=	ENSP00000332247.2:p.Met411=
ENST00000504192.2:c.841A=	ENSP00000443441.1:p.Met281=
ENST00000536426.1:n.248A=
ENST00000545059.5:n.3867A=
NM_012463.3:c.1231A=	NP_036595.2:p.Met411=
XM_005253563.1:c.1231A=	XP_005253620.1:p.Met411=
XM_006719317.2:c.718A=	XP_006719380.1:p.Met240=
XM_006719318.2:c.409A=	XP_006719381.1:p.Met137=
XR_429088.1:n.1394A=
XM_024448910.1:c.1231A=	XP_024304678.1:p.Met411=
XM_024448911.1:c.718A=	XP_024304679.1:p.Met240=
XM_024448912.1:c.409A=	XP_024304680.1:p.Met137=
NM_012463.4:c.1231A= MANE Select	NP_036595.2:p.Met411=