Canonical Allele Identifier: CA2062807359
Gene: ATP2A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110343474_110343475delinsAT , CM000674.2:g.110343474_110343475delinsAT GRCh38
NC_000012.11:g.110781279_110781280delinsAT , CM000674.1:g.110781279_110781280delinsAT GRCh37
NC_000012.10:g.109265662_109265663delinsAT NCBI36
NG_007097.2:g.66848_66849delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.2521+40_2521+41delinsAT MANE Select ENSP00000440045.2:n.2521+40_2521+41delinsAT
ENST00000308664.10:c.2521+40_2521+41delinsAT ENSP00000311186.6:n.2521+40_2521+41delinsAT
ENST00000377685.9:c.*2361+40_*2361+41delinsAT ENSP00000366913.4:n.*2361+40_*2361+41delinsAT
ENST00000539276.6:c.2521+40_2521+41delinsAT ENSP00000440045.2:n.2521+40_2521+41delinsAT
ENST00000547792.1:n.179+40_179+41delinsAT
ENST00000548169.2:c.2192+40_2192+41delinsAT
NM_001681.3:c.2521+40_2521+41delinsAT NP_001672.1:n.2521+40_2521+41delinsAT
NM_170665.3:c.2521+40_2521+41delinsAT NP_733765.1:n.2521+40_2521+41delinsAT
XM_005253888.1:c.2521+40_2521+41delinsAT XP_005253945.1:n.2521+40_2521+41delinsAT
XM_011538402.1:c.2521+40_2521+41delinsAT XP_011536704.1:n.2521+40_2521+41delinsAT
XM_011538403.1:c.2521+40_2521+41delinsAT XP_011536705.1:n.2521+40_2521+41delinsAT
XR_243009.1:n.2527+40_2527+41delinsAT
XM_005253888.3:c.2521+40_2521+41delinsAT XP_005253945.1:n.2521+40_2521+41delinsAT
XM_011538402.3:c.2521+40_2521+41delinsAT XP_011536704.1:n.2521+40_2521+41delinsAT
XR_002957329.1:n.2527+40_2527+41delinsAT
XR_243009.3:n.2527+40_2527+41delinsAT
NM_170665.4:c.2521+40_2521+41delinsAT MANE Select NP_733765.1:n.2521+40_2521+41delinsAT
NM_001681.4:c.2521+40_2521+41delinsAT NP_001672.1:n.2521+40_2521+41delinsAT