Canonical Allele Identifier: CA951739506
Gene: ATP2A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110345180_110345181dup , CM000674.2:g.110345180_110345181dup GRCh38
NC_000012.11:g.110782985_110782986dup , CM000674.1:g.110782985_110782986dup GRCh37
NC_000012.10:g.109267368_109267369dup NCBI36
NG_007097.2:g.68554_68555dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.2608-69_2608-68dup MANE Select ENSP00000440045.2:n.2608-69_2608-68dup
ENST00000308664.10:c.2608-69_2608-68dup ENSP00000311186.6:n.2608-69_2608-68dup
ENST00000377685.9:c.*2448-69_*2448-68dup ENSP00000366913.4:n.*2448-69_*2448-68dup
ENST00000539276.6:c.2608-69_2608-68dup ENSP00000440045.2:n.2608-69_2608-68dup
ENST00000547792.1:n.474_475dup
ENST00000548169.2:c.2279-69_2279-68dup
NM_001681.3:c.2608-69_2608-68dup NP_001672.1:n.2608-69_2608-68dup
NM_170665.3:c.2608-69_2608-68dup NP_733765.1:n.2608-69_2608-68dup
XM_005253888.1:c.2608-69_2608-68dup XP_005253945.1:n.2608-69_2608-68dup
XM_011538402.1:c.2608-69_2608-68dup XP_011536704.1:n.2608-69_2608-68dup
XR_243009.1:n.2614-69_2614-68dup
XM_005253888.3:c.2608-69_2608-68dup XP_005253945.1:n.2608-69_2608-68dup
XM_011538402.3:c.2608-69_2608-68dup XP_011536704.1:n.2608-69_2608-68dup
XR_002957329.1:n.2614-69_2614-68dup
XR_243009.3:n.2614-69_2614-68dup
NM_170665.4:c.2608-69_2608-68dup MANE Select NP_733765.1:n.2608-69_2608-68dup
NM_001681.4:c.2608-69_2608-68dup NP_001672.1:n.2608-69_2608-68dup