Canonical Allele Identifier: CA2062805036

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110340954_110340955delinsTC , CM000674.2:g.110340954_110340955delinsTC	GRCh38
NC_000012.11:g.110778759_110778760delinsTC , CM000674.1:g.110778759_110778760delinsTC	GRCh37
NC_000012.10:g.109263142_109263143delinsTC	NCBI36
NG_007097.2:g.64328_64329delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2057_2058delinsTC MANE Select	ENSP00000440045.2:p.Ile686=
ENST00000308664.10:c.2057_2058delinsTC	ENSP00000311186.6:p.Ile686=
ENST00000377685.9:c.*1897_*1898delinsTC	ENSP00000366913.4:n.*1897_*1898delinsTC
ENST00000539276.6:c.2057_2058delinsTC	ENSP00000440045.2:p.Ile686=
ENST00000548169.2:c.1728_1729delinsTC
NM_001681.3:c.2057_2058delinsTC	NP_001672.1:p.Ile686=
NM_170665.3:c.2057_2058delinsTC	NP_733765.1:p.Ile686=
XM_005253888.1:c.2057_2058delinsTC	XP_005253945.1:p.Ile686=
XM_011538402.1:c.2057_2058delinsTC	XP_011536704.1:p.Ile686=
XM_011538403.1:c.2057_2058delinsTC	XP_011536705.1:p.Ile686=
XR_243009.1:n.2063_2064delinsTC
XM_005253888.3:c.2057_2058delinsTC	XP_005253945.1:p.Ile686=
XM_011538402.3:c.2057_2058delinsTC	XP_011536704.1:p.Ile686=
XR_002957329.1:n.2063_2064delinsTC
XR_243009.3:n.2063_2064delinsTC
NM_170665.4:c.2057_2058delinsTC MANE Select	NP_733765.1:p.Ile686=
NM_001681.4:c.2057_2058delinsTC	NP_001672.1:p.Ile686=