Canonical Allele Identifier: CA2238618409
Gene: ATP2C2 HGNC NCBI

Linked Data

dbSNP Id: rs1906483078

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84412702dup , CM000678.2:g.84412702dup GRCh38
NC_000016.9:g.84446308dup , CM000678.1:g.84446308dup GRCh37
NC_000016.8:g.83003809dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262429.9:c.515+1937dup MANE Select ENSP00000262429.4:n.515+1937dup
ENST00000262429.8:c.515+1937dup ENSP00000262429.4:n.515+1937dup
ENST00000416219.6:c.515+1937dup ENSP00000397925.2:n.515+1937dup
ENST00000420010.6:n.188+2099dup
ENST00000565546.5:n.250+1937dup
ENST00000565631.5:n.1006+1937dup
ENST00000565927.1:n.504+1937dup
ENST00000569207.5:c.237+1937dup
NM_001286527.2:c.515+1937dup NP_001273456.2:n.515+1937dup
NM_001291454.1:c.62+2099dup NP_001278383.1:n.62+2099dup
NM_014861.3:c.515+1937dup NP_055676.3:n.515+1937dup
XM_011523486.1:c.446+1937dup XP_011521788.1:n.446+1937dup
XM_011523486.2:c.446+1937dup XP_011521788.1:n.446+1937dup
XR_001752045.1:n.608+1937dup
NM_001286527.3:c.515+1937dup NP_001273456.2:n.515+1937dup
NM_001291454.2:c.62+2099dup NP_001278383.1:n.62+2099dup
NM_014861.4:c.515+1937dup MANE Select NP_055676.3:n.515+1937dup