Canonical Allele Identifier: CA387157542

Gene: ATP6V0A2

Linked Data

• COSMIC: COSM936488
• MyVariant Identifiers: chr12:g.124229211G>A (hg19) ; chr12:g.123744664G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744664G>A , CM000674.2:g.123744664G>A	GRCh38
NC_000012.11:g.124229211G>A , CM000674.1:g.124229211G>A	GRCh37
NC_000012.10:g.122795164G>A	NCBI36
NG_012743.1:g.37347G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1394G>A MANE Select	ENSP00000332247.2:p.Gly465Asp
ENST00000540368.6:n.1425G>A
ENST00000674794.1:c.1482G>A
ENST00000675260.1:n.669G>A
ENST00000675344.1:c.*415G>A	ENSP00000501953.1:n.*415G>A
ENST00000330342.7:c.1394G>A	ENSP00000332247.2:p.Gly465Asp
ENST00000536426.1:n.411G>A
ENST00000545059.5:n.4030G>A
NM_012463.3:c.1394G>A	NP_036595.2:p.Gly465Asp
XM_005253563.1:c.1394G>A	XP_005253620.1:p.Gly465Asp
XM_006719317.2:c.881G>A	XP_006719380.1:p.Gly294Asp
XM_006719318.2:c.572G>A	XP_006719381.1:p.Gly191Asp
XR_429088.1:n.1557G>A
XM_024448910.1:c.1394G>A	XP_024304678.1:p.Gly465Asp
XM_024448911.1:c.881G>A	XP_024304679.1:p.Gly294Asp
XM_024448912.1:c.572G>A	XP_024304680.1:p.Gly191Asp
NM_012463.4:c.1394G>A MANE Select	NP_036595.2:p.Gly465Asp