Canonical Allele Identifier: CA482452322

Gene: ATP6V0A2

Linked Data

• COSMIC: COSM6136030
• MyVariant Identifiers: chr12:g.124229215C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744668C>G , CM000674.2:g.123744668C>G	GRCh38
NC_000012.11:g.124229215C>G , CM000674.1:g.124229215C>G	GRCh37
NC_000012.10:g.122795168C>G	NCBI36
NG_012743.1:g.37351C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1398C>G MANE Select	ENSP00000332247.2:p.Leu466=
ENST00000540368.6:n.1429C>G
ENST00000674794.1:c.1486C>G
ENST00000675260.1:n.673C>G
ENST00000675344.1:c.*419C>G	ENSP00000501953.1:n.*419C>G
ENST00000330342.7:c.1398C>G	ENSP00000332247.2:p.Leu466=
ENST00000536426.1:n.415C>G
ENST00000545059.5:n.4034C>G
NM_012463.3:c.1398C>G	NP_036595.2:p.Leu466=
XM_005253563.1:c.1398C>G	XP_005253620.1:p.Leu466=
XM_006719317.2:c.885C>G	XP_006719380.1:p.Leu295=
XM_006719318.2:c.576C>G	XP_006719381.1:p.Leu192=
XR_429088.1:n.1561C>G
XM_024448910.1:c.1398C>G	XP_024304678.1:p.Leu466=
XM_024448911.1:c.885C>G	XP_024304679.1:p.Leu295=
XM_024448912.1:c.576C>G	XP_024304680.1:p.Leu192=
NM_012463.4:c.1398C>G MANE Select	NP_036595.2:p.Leu466=