Canonical Allele Identifier: CA387156372

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124228784C>A (hg19) ; chr12:g.123744237C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744237C>A , CM000674.2:g.123744237C>A	GRCh38
NC_000012.11:g.124228784C>A , CM000674.1:g.124228784C>A	GRCh37
NC_000012.10:g.122794737C>A	NCBI36
NG_012743.1:g.36920C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1226C>A MANE Select	ENSP00000332247.2:p.Ala409Asp
ENST00000540368.6:n.1257C>A
ENST00000674794.1:c.1314C>A
ENST00000675260.1:n.501C>A
ENST00000675344.1:c.*247C>A	ENSP00000501953.1:n.*247C>A
ENST00000330342.7:c.1226C>A	ENSP00000332247.2:p.Ala409Asp
ENST00000504192.2:c.836C>A	ENSP00000443441.1:p.Ala279Asp
ENST00000536426.1:n.243C>A
ENST00000545059.5:n.3862C>A
NM_012463.3:c.1226C>A	NP_036595.2:p.Ala409Asp
XM_005253563.1:c.1226C>A	XP_005253620.1:p.Ala409Asp
XM_006719317.2:c.713C>A	XP_006719380.1:p.Ala238Asp
XM_006719318.2:c.404C>A	XP_006719381.1:p.Ala135Asp
XR_429088.1:n.1389C>A
XM_024448910.1:c.1226C>A	XP_024304678.1:p.Ala409Asp
XM_024448911.1:c.713C>A	XP_024304679.1:p.Ala238Asp
XM_024448912.1:c.404C>A	XP_024304680.1:p.Ala135Asp
NM_012463.4:c.1226C>A MANE Select	NP_036595.2:p.Ala409Asp