Canonical Allele Identifier: CA6861730

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123735572A>G , CM000674.2:g.123735572A>G	GRCh38
NC_000012.11:g.124220119A>G , CM000674.1:g.124220119A>G	GRCh37
NC_000012.10:g.122786072A>G	NCBI36
NG_012743.1:g.28255A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_012463.4:c.773A>G MANE Select	NP_036595.2:p.Glu258Gly
ENST00000330342.8:c.773A>G MANE Select	ENSP00000332247.2:p.Glu258Gly
NM_012463.3:c.773A>G	NP_036595.2:p.Glu258Gly
ENST00000330342.7:c.773A>G	ENSP00000332247.2:p.Glu258Gly
ENST00000504192.2:c.383A>G	ENSP00000443441.1:p.Glu128Gly
ENST00000540368.5:n.983A>G
ENST00000540368.6:n.804A>G
ENST00000545059.5:n.3409A>G
ENST00000613625.4:c.773A>G	ENSP00000482236.1:p.Glu258Gly
ENST00000613625.5:c.773A>G	ENSP00000482236.1:p.Glu258Gly
ENST00000674794.1:c.213A>G
ENST00000675344.1:c.773A>G	ENSP00000501953.1:p.Glu258Gly
XM_005253563.1:c.773A>G	XP_005253620.1:p.Glu258Gly
XM_006719317.2:c.260A>G	XP_006719380.1:p.Glu87Gly
XM_024448910.1:c.773A>G	XP_024304678.1:p.Glu258Gly
XM_024448911.1:c.260A>G	XP_024304679.1:p.Glu87Gly
XR_429088.1:n.936A>G