Canonical Allele Identifier: CA482271356

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123751127G>A , CM000674.2:g.123751127G>A	GRCh38
NC_000012.11:g.124235674G>A , CM000674.1:g.124235674G>A	GRCh37
NC_000012.10:g.122801627G>A	NCBI36
NG_012743.1:g.43810G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012463.4:c.1953G>A MANE Select	NP_036595.2:p.Val651=
ENST00000330342.8:c.1953G>A MANE Select	ENSP00000332247.2:p.Val651=
NM_012463.3:c.1953G>A	NP_036595.2:p.Val651=
ENST00000330342.7:c.1953G>A	ENSP00000332247.2:p.Val651=
ENST00000534943.5:c.-208G>A	ENSP00000443726.1:n.-208G>A
ENST00000540368.6:n.1984G>A
ENST00000674794.1:c.2041G>A
ENST00000675260.1:n.1228G>A
ENST00000675344.1:c.*974G>A	ENSP00000501953.1:n.*974G>A
XM_005253563.1:c.1936-1156G>A	XP_005253620.1:n.1936-1156G>A
XM_006719317.2:c.1440G>A	XP_006719380.1:p.Val480=
XM_006719318.2:c.1131G>A	XP_006719381.1:p.Val377=
XM_024448910.1:c.1936-1156G>A	XP_024304678.1:n.1936-1156G>A
XM_024448911.1:c.1440G>A	XP_024304679.1:p.Val480=
XM_024448912.1:c.1131G>A	XP_024304680.1:p.Val377=
XR_429088.1:n.2116G>A