Canonical Allele Identifier: CA2573332532
Gene: ATP2A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110342310_110342311insTAC , CM000674.2:g.110342310_110342311insTAC GRCh38
NC_000012.11:g.110780115_110780116insTAC , CM000674.1:g.110780115_110780116insTAC GRCh37
NC_000012.10:g.109264498_109264499insTAC NCBI36
NG_007097.2:g.65684_65685insTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.2180_2181insTAC MANE Select ENSP00000440045.2:p.Lys727delinsAsnThr
ENST00000308664.10:c.2180_2181insTAC ENSP00000311186.6:p.Lys727delinsAsnThr
ENST00000377685.9:c.*2020_*2021insTAC ENSP00000366913.4:n.*2020_*2021insTAC
ENST00000539276.6:c.2180_2181insTAC ENSP00000440045.2:p.Lys727delinsAsnThr
ENST00000548169.2:c.1851_1852insTAC
NM_001681.3:c.2180_2181insTAC NP_001672.1:p.Lys727delinsAsnThr
NM_170665.3:c.2180_2181insTAC NP_733765.1:p.Lys727delinsAsnThr
XM_005253888.1:c.2180_2181insTAC XP_005253945.1:p.Lys727delinsAsnThr
XM_011538402.1:c.2180_2181insTAC XP_011536704.1:p.Lys727delinsAsnThr
XM_011538403.1:c.2180_2181insTAC XP_011536705.1:p.Lys727delinsAsnThr
XR_243009.1:n.2186_2187insTAC
XM_005253888.3:c.2180_2181insTAC XP_005253945.1:p.Lys727delinsAsnThr
XM_011538402.3:c.2180_2181insTAC XP_011536704.1:p.Lys727delinsAsnThr
XR_002957329.1:n.2186_2187insTAC
XR_243009.3:n.2186_2187insTAC
NM_170665.4:c.2180_2181insTAC MANE Select NP_733765.1:p.Lys727delinsAsnThr
NM_001681.4:c.2180_2181insTAC NP_001672.1:p.Lys727delinsAsnThr