Canonical Allele Identifier: CA482270900

Gene: ATP6V0A2

Linked Data

• gnomAD v4: 12-123743925-A-G
• MyVariant Identifiers: chr12:g.124228472A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123743925A>G , CM000674.2:g.123743925A>G	GRCh38
NC_000012.11:g.124228472A>G , CM000674.1:g.124228472A>G	GRCh37
NC_000012.10:g.122794425A>G	NCBI36
NG_012743.1:g.36608A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1179A>G MANE Select	ENSP00000332247.2:p.Glu393=
ENST00000540368.6:n.1210A>G
ENST00000674794.1:c.1267A>G
ENST00000675260.1:n.454A>G
ENST00000675344.1:c.*200A>G	ENSP00000501953.1:n.*200A>G
ENST00000330342.7:c.1179A>G	ENSP00000332247.2:p.Glu393=
ENST00000504192.2:c.789A>G	ENSP00000443441.1:p.Glu263=
ENST00000536426.1:n.196A>G
ENST00000545059.5:n.3815A>G
NM_012463.3:c.1179A>G	NP_036595.2:p.Glu393=
XM_005253563.1:c.1179A>G	XP_005253620.1:p.Glu393=
XM_006719317.2:c.666A>G	XP_006719380.1:p.Glu222=
XM_006719318.2:c.357A>G	XP_006719381.1:p.Glu119=
XR_429088.1:n.1342A>G
XM_024448910.1:c.1179A>G	XP_024304678.1:p.Glu393=
XM_024448911.1:c.666A>G	XP_024304679.1:p.Glu222=
XM_024448912.1:c.357A>G	XP_024304680.1:p.Glu119=
NM_012463.4:c.1179A>G MANE Select	NP_036595.2:p.Glu393=