Canonical Allele Identifier: CA387157541

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124229210G>T (hg19) ; chr12:g.123744663G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744663G>T , CM000674.2:g.123744663G>T	GRCh38
NC_000012.11:g.124229210G>T , CM000674.1:g.124229210G>T	GRCh37
NC_000012.10:g.122795163G>T	NCBI36
NG_012743.1:g.37346G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1393G>T MANE Select	ENSP00000332247.2:p.Gly465Cys
ENST00000540368.6:n.1424G>T
ENST00000674794.1:c.1481G>T
ENST00000675260.1:n.668G>T
ENST00000675344.1:c.*414G>T	ENSP00000501953.1:n.*414G>T
ENST00000330342.7:c.1393G>T	ENSP00000332247.2:p.Gly465Cys
ENST00000536426.1:n.410G>T
ENST00000545059.5:n.4029G>T
NM_012463.3:c.1393G>T	NP_036595.2:p.Gly465Cys
XM_005253563.1:c.1393G>T	XP_005253620.1:p.Gly465Cys
XM_006719317.2:c.880G>T	XP_006719380.1:p.Gly294Cys
XM_006719318.2:c.571G>T	XP_006719381.1:p.Gly191Cys
XR_429088.1:n.1556G>T
XM_024448910.1:c.1393G>T	XP_024304678.1:p.Gly465Cys
XM_024448911.1:c.880G>T	XP_024304679.1:p.Gly294Cys
XM_024448912.1:c.571G>T	XP_024304680.1:p.Gly191Cys
NM_012463.4:c.1393G>T MANE Select	NP_036595.2:p.Gly465Cys