Canonical Allele Identifier: CA387155517

Gene: ATP6V0A2

Linked Data

• gnomAD v4: 12-123743842-C-G
• MyVariant Identifiers: chr12:g.124228389C>G (hg19) ; chr12:g.123743842C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123743842C>G , CM000674.2:g.123743842C>G	GRCh38
NC_000012.11:g.124228389C>G , CM000674.1:g.124228389C>G	GRCh37
NC_000012.10:g.122794342C>G	NCBI36
NG_012743.1:g.36525C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1096C>G MANE Select	ENSP00000332247.2:p.Pro366Ala
ENST00000540368.6:n.1127C>G
ENST00000674794.1:c.1184C>G
ENST00000675260.1:n.371C>G
ENST00000675344.1:c.*117C>G	ENSP00000501953.1:n.*117C>G
ENST00000330342.7:c.1096C>G	ENSP00000332247.2:p.Pro366Ala
ENST00000504192.2:c.706C>G	ENSP00000443441.1:p.Pro236Ala
ENST00000536426.1:n.113C>G
ENST00000545059.5:n.3732C>G
NM_012463.3:c.1096C>G	NP_036595.2:p.Pro366Ala
XM_005253563.1:c.1096C>G	XP_005253620.1:p.Pro366Ala
XM_006719317.2:c.583C>G	XP_006719380.1:p.Pro195Ala
XM_006719318.2:c.274C>G	XP_006719381.1:p.Pro92Ala
XR_429088.1:n.1259C>G
XM_024448910.1:c.1096C>G	XP_024304678.1:p.Pro366Ala
XM_024448911.1:c.583C>G	XP_024304679.1:p.Pro195Ala
XM_024448912.1:c.274C>G	XP_024304680.1:p.Pro92Ala
NM_012463.4:c.1096C>G MANE Select	NP_036595.2:p.Pro366Ala