Canonical Allele Identifier: CA2540669559
Gene: ATP2A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110345476_110345477insT , CM000674.2:g.110345476_110345477insT GRCh38
NC_000012.11:g.110783281_110783282insT , CM000674.1:g.110783281_110783282insT GRCh37
NC_000012.10:g.109267664_109267665insT NCBI36
NG_007097.2:g.68850_68851insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.2741+94_2741+95insT MANE Select ENSP00000440045.2:n.2741+94_2741+95insT
ENST00000308664.10:c.2741+94_2741+95insT ENSP00000311186.6:n.2741+94_2741+95insT
ENST00000313432.5:n.40_41insT
ENST00000377685.9:c.*2581+94_*2581+95insT ENSP00000366913.4:n.*2581+94_*2581+95insT
ENST00000539276.6:c.2741+94_2741+95insT ENSP00000440045.2:n.2741+94_2741+95insT
ENST00000548169.2:c.2412+94_2412+95insT
NM_001681.3:c.2741+94_2741+95insT NP_001672.1:n.2741+94_2741+95insT
NM_170665.3:c.2741+94_2741+95insT NP_733765.1:n.2741+94_2741+95insT
XM_005253888.1:c.2741+94_2741+95insT XP_005253945.1:n.2741+94_2741+95insT
XM_011538402.1:c.2741+94_2741+95insT XP_011536704.1:n.2741+94_2741+95insT
XR_243009.1:n.2747+94_2747+95insT
XM_005253888.3:c.2741+94_2741+95insT XP_005253945.1:n.2741+94_2741+95insT
XM_011538402.3:c.2741+94_2741+95insT XP_011536704.1:n.2741+94_2741+95insT
XR_002957329.1:n.2747+94_2747+95insT
XR_243009.3:n.2747+94_2747+95insT
NM_170665.4:c.2741+94_2741+95insT MANE Select NP_733765.1:n.2741+94_2741+95insT
NM_001681.4:c.2741+94_2741+95insT NP_001672.1:n.2741+94_2741+95insT