Canonical Allele Identifier: CA2830554317
Gene: ATP2A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110345083dup , CM000674.2:g.110345083dup GRCh38
NC_000012.11:g.110782888dup , CM000674.1:g.110782888dup GRCh37
NC_000012.10:g.109267271dup NCBI36
NG_007097.2:g.68457dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.2607+112dup MANE Select ENSP00000440045.2:n.2607+112dup
ENST00000308664.10:c.2607+112dup ENSP00000311186.6:n.2607+112dup
ENST00000377685.9:c.*2447+112dup ENSP00000366913.4:n.*2447+112dup
ENST00000539276.6:c.2607+112dup ENSP00000440045.2:n.2607+112dup
ENST00000547792.1:n.377dup
ENST00000548169.2:c.2278+112dup
NM_001681.3:c.2607+112dup NP_001672.1:n.2607+112dup
NM_170665.3:c.2607+112dup NP_733765.1:n.2607+112dup
XM_005253888.1:c.2607+112dup XP_005253945.1:n.2607+112dup
XM_011538402.1:c.2607+112dup XP_011536704.1:n.2607+112dup
XR_243009.1:n.2613+112dup
XM_005253888.3:c.2607+112dup XP_005253945.1:n.2607+112dup
XM_011538402.3:c.2607+112dup XP_011536704.1:n.2607+112dup
XR_002957329.1:n.2613+112dup
XR_243009.3:n.2613+112dup
NM_170665.4:c.2607+112dup MANE Select NP_733765.1:n.2607+112dup
NM_001681.4:c.2607+112dup NP_001672.1:n.2607+112dup