Canonical Allele Identifier: CA387156649

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124228831G>T (hg19) ; chr12:g.123744284G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744284G>T , CM000674.2:g.123744284G>T	GRCh38
NC_000012.11:g.124228831G>T , CM000674.1:g.124228831G>T	GRCh37
NC_000012.10:g.122794784G>T	NCBI36
NG_012743.1:g.36967G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1273G>T MANE Select	ENSP00000332247.2:p.Ala425Ser
ENST00000540368.6:n.1304G>T
ENST00000674794.1:c.1361G>T
ENST00000675260.1:n.548G>T
ENST00000675344.1:c.*294G>T	ENSP00000501953.1:n.*294G>T
ENST00000330342.7:c.1273G>T	ENSP00000332247.2:p.Ala425Ser
ENST00000504192.2:c.883G>T	ENSP00000443441.1:p.Ala295Ser
ENST00000536426.1:n.290G>T
ENST00000545059.5:n.3909G>T
NM_012463.3:c.1273G>T	NP_036595.2:p.Ala425Ser
XM_005253563.1:c.1273G>T	XP_005253620.1:p.Ala425Ser
XM_006719317.2:c.760G>T	XP_006719380.1:p.Ala254Ser
XM_006719318.2:c.451G>T	XP_006719381.1:p.Ala151Ser
XR_429088.1:n.1436G>T
XM_024448910.1:c.1273G>T	XP_024304678.1:p.Ala425Ser
XM_024448911.1:c.760G>T	XP_024304679.1:p.Ala254Ser
XM_024448912.1:c.451G>T	XP_024304680.1:p.Ala151Ser
NM_012463.4:c.1273G>T MANE Select	NP_036595.2:p.Ala425Ser