Canonical Allele Identifier: CA2062810472

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345639_110345640delinsCT , CM000674.2:g.110345639_110345640delinsCT	GRCh38
NC_000012.11:g.110783444_110783445delinsCT , CM000674.1:g.110783444_110783445delinsCT	GRCh37
NC_000012.10:g.109267827_109267828delinsCT	NCBI36
NG_007097.2:g.69013_69014delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2741+257_2741+258delinsCT MANE Select	ENSP00000440045.2:n.2741+257_2741+258delinsCT
ENST00000308664.10:c.2741+257_2741+258delinsCT	ENSP00000311186.6:n.2741+257_2741+258delinsCT
ENST00000313432.5:n.203_204delinsCT
ENST00000377685.9:c.*2581+257_*2581+258delinsCT	ENSP00000366913.4:n.*2581+257_*2581+258delinsCT
ENST00000539276.6:c.2741+257_2741+258delinsCT	ENSP00000440045.2:n.2741+257_2741+258delinsCT
ENST00000548169.2:c.2412+257_2412+258delinsCT
NM_001681.3:c.2741+257_2741+258delinsCT	NP_001672.1:n.2741+257_2741+258delinsCT
NM_170665.3:c.2741+257_2741+258delinsCT	NP_733765.1:n.2741+257_2741+258delinsCT
XM_005253888.1:c.2741+257_2741+258delinsCT	XP_005253945.1:n.2741+257_2741+258delinsCT
XM_011538402.1:c.2741+257_2741+258delinsCT	XP_011536704.1:n.2741+257_2741+258delinsCT
XR_243009.1:n.2747+257_2747+258delinsCT
XM_005253888.3:c.2741+257_2741+258delinsCT	XP_005253945.1:n.2741+257_2741+258delinsCT
XM_011538402.3:c.2741+257_2741+258delinsCT	XP_011536704.1:n.2741+257_2741+258delinsCT
XR_002957329.1:n.2747+257_2747+258delinsCT
XR_243009.3:n.2747+257_2747+258delinsCT
NM_170665.4:c.2741+257_2741+258delinsCT MANE Select	NP_733765.1:n.2741+257_2741+258delinsCT
NM_001681.4:c.2741+257_2741+258delinsCT	NP_001672.1:n.2741+257_2741+258delinsCT