Canonical Allele Identifier: CA387152943

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123733956A>G , CM000674.2:g.123733956A>G	GRCh38
NC_000012.11:g.124218503A>G , CM000674.1:g.124218503A>G	GRCh37
NC_000012.10:g.122784456A>G	NCBI36
NG_012743.1:g.26639A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.679A>G MANE Select	ENSP00000332247.2:p.Ile227Val
ENST00000540368.6:n.710A>G
ENST00000613625.5:c.679A>G	ENSP00000482236.1:p.Ile227Val
ENST00000674794.1:c.119A>G
ENST00000675344.1:c.679A>G	ENSP00000501953.1:p.Ile227Val
ENST00000330342.7:c.679A>G	ENSP00000332247.2:p.Ile227Val
ENST00000504192.2:c.289A>G	ENSP00000443441.1:p.Ile97Val
ENST00000540368.5:n.889A>G
ENST00000545059.5:n.3315A>G
ENST00000613625.4:c.679A>G	ENSP00000482236.1:p.Ile227Val
NM_012463.3:c.679A>G	NP_036595.2:p.Ile227Val
XM_005253563.1:c.679A>G	XP_005253620.1:p.Ile227Val
XM_006719317.2:c.166A>G	XP_006719380.1:p.Ile56Val
XR_429088.1:n.842A>G
XM_024448910.1:c.679A>G	XP_024304678.1:p.Ile227Val
XM_024448911.1:c.166A>G	XP_024304679.1:p.Ile56Val
NM_012463.4:c.679A>G MANE Select	NP_036595.2:p.Ile227Val