Canonical Allele Identifier: CA386913037

Gene: ATP2A2

Linked Data

• MyVariant Identifiers: chr12:g.110720602T>A (hg19) ; chr12:g.110282797T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110282797T>A , CM000674.2:g.110282797T>A	GRCh38
NC_000012.11:g.110720602T>A , CM000674.1:g.110720602T>A	GRCh37
NC_000012.10:g.109204985T>A	NCBI36
NG_007097.2:g.6171T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000552636.2:c.-157+2T>A	ENSP00000447406.2:n.-157+2T>A
ENST00000539276.7:c.219+2T>A MANE Select	ENSP00000440045.2:n.219+2T>A
ENST00000308664.10:c.219+2T>A	ENSP00000311186.6:n.219+2T>A
ENST00000377685.9:c.*59+2T>A	ENSP00000366913.4:n.*59+2T>A
ENST00000539276.6:c.219+2T>A	ENSP00000440045.2:n.219+2T>A
ENST00000552636.1:c.-83+2T>A	ENSP00000447406.1:n.-83+2T>A
NM_001681.3:c.219+2T>A	NP_001672.1:n.219+2T>A
NM_170665.3:c.219+2T>A	NP_733765.1:n.219+2T>A
XM_005253888.1:c.219+2T>A	XP_005253945.1:n.219+2T>A
XM_011538402.1:c.219+2T>A	XP_011536704.1:n.219+2T>A
XM_011538403.1:c.219+2T>A	XP_011536705.1:n.219+2T>A
XR_243009.1:n.225+2T>A
XM_005253888.3:c.219+2T>A	XP_005253945.1:n.219+2T>A
XM_011538402.3:c.219+2T>A	XP_011536704.1:n.219+2T>A
XR_002957329.1:n.225+2T>A
XR_243009.3:n.225+2T>A
NM_170665.4:c.219+2T>A MANE Select	NP_733765.1:n.219+2T>A
NM_001681.4:c.219+2T>A	NP_001672.1:n.219+2T>A