Canonical Allele Identifier: CA387156609

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124228822T>G (hg19) ; chr12:g.123744275T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744275T>G , CM000674.2:g.123744275T>G	GRCh38
NC_000012.11:g.124228822T>G , CM000674.1:g.124228822T>G	GRCh37
NC_000012.10:g.122794775T>G	NCBI36
NG_012743.1:g.36958T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1264T>G MANE Select	ENSP00000332247.2:p.Phe422Val
ENST00000540368.6:n.1295T>G
ENST00000674794.1:c.1352T>G
ENST00000675260.1:n.539T>G
ENST00000675344.1:c.*285T>G	ENSP00000501953.1:n.*285T>G
ENST00000330342.7:c.1264T>G	ENSP00000332247.2:p.Phe422Val
ENST00000504192.2:c.874T>G	ENSP00000443441.1:p.Phe292Val
ENST00000536426.1:n.281T>G
ENST00000545059.5:n.3900T>G
NM_012463.3:c.1264T>G	NP_036595.2:p.Phe422Val
XM_005253563.1:c.1264T>G	XP_005253620.1:p.Phe422Val
XM_006719317.2:c.751T>G	XP_006719380.1:p.Phe251Val
XM_006719318.2:c.442T>G	XP_006719381.1:p.Phe148Val
XR_429088.1:n.1427T>G
XM_024448910.1:c.1264T>G	XP_024304678.1:p.Phe422Val
XM_024448911.1:c.751T>G	XP_024304679.1:p.Phe251Val
XM_024448912.1:c.442T>G	XP_024304680.1:p.Phe148Val
NM_012463.4:c.1264T>G MANE Select	NP_036595.2:p.Phe422Val