Canonical Allele Identifier: CA2062804761
Gene: ATP2A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110340772G= , CM000674.2:g.110340772G= GRCh38
NC_000012.11:g.110778577G= , CM000674.1:g.110778577G= GRCh37
NC_000012.10:g.109262960G= NCBI36
NG_007097.2:g.64146G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.1875G= MANE Select ENSP00000440045.2:p.Gly625=
ENST00000308664.10:c.1875G= ENSP00000311186.6:p.Gly625=
ENST00000377685.9:c.*1715G= ENSP00000366913.4:n.*1715G=
ENST00000539276.6:c.1875G= ENSP00000440045.2:p.Gly625=
ENST00000548169.2:c.1546G=
NM_001681.3:c.1875G= NP_001672.1:p.Gly625=
NM_170665.3:c.1875G= NP_733765.1:p.Gly625=
XM_005253888.1:c.1875G= XP_005253945.1:p.Gly625=
XM_011538402.1:c.1875G= XP_011536704.1:p.Gly625=
XM_011538403.1:c.1875G= XP_011536705.1:p.Gly625=
XR_243009.1:n.1881G=
XM_005253888.3:c.1875G= XP_005253945.1:p.Gly625=
XM_011538402.3:c.1875G= XP_011536704.1:p.Gly625=
XR_002957329.1:n.1881G=
XR_243009.3:n.1881G=
NM_170665.4:c.1875G= MANE Select NP_733765.1:p.Gly625=
NM_001681.4:c.1875G= NP_001672.1:p.Gly625=