Canonical Allele Identifier: CA2062806177
Gene: ATP2A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110342290C= , CM000674.2:g.110342290C= GRCh38
NC_000012.11:g.110780095C= , CM000674.1:g.110780095C= GRCh37
NC_000012.10:g.109264478C= NCBI36
NG_007097.2:g.65664C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.2160C= MANE Select ENSP00000440045.2:p.Gly720=
ENST00000308664.10:c.2160C= ENSP00000311186.6:p.Gly720=
ENST00000377685.9:c.*2000C= ENSP00000366913.4:n.*2000C=
ENST00000539276.6:c.2160C= ENSP00000440045.2:p.Gly720=
ENST00000548169.2:c.1831C=
NM_001681.3:c.2160C= NP_001672.1:p.Gly720=
NM_170665.3:c.2160C= NP_733765.1:p.Gly720=
XM_005253888.1:c.2160C= XP_005253945.1:p.Gly720=
XM_011538402.1:c.2160C= XP_011536704.1:p.Gly720=
XM_011538403.1:c.2160C= XP_011536705.1:p.Gly720=
XR_243009.1:n.2166C=
XM_005253888.3:c.2160C= XP_005253945.1:p.Gly720=
XM_011538402.3:c.2160C= XP_011536704.1:p.Gly720=
XR_002957329.1:n.2166C=
XR_243009.3:n.2166C=
NM_170665.4:c.2160C= MANE Select NP_733765.1:p.Gly720=
NM_001681.4:c.2160C= NP_001672.1:p.Gly720=