Canonical Allele Identifier: CA2620870426
Gene: ATP2A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110345422_110345424dup , CM000674.2:g.110345422_110345424dup GRCh38
NC_000012.11:g.110783227_110783229dup , CM000674.1:g.110783227_110783229dup GRCh37
NC_000012.10:g.109267610_109267612dup NCBI36
NG_007097.2:g.68796_68798dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.2741+40_2741+42dup MANE Select ENSP00000440045.2:n.2741+40_2741+42dup
ENST00000308664.10:c.2741+40_2741+42dup ENSP00000311186.6:n.2741+40_2741+42dup
ENST00000377685.9:c.*2581+40_*2581+42dup ENSP00000366913.4:n.*2581+40_*2581+42dup
ENST00000539276.6:c.2741+40_2741+42dup ENSP00000440045.2:n.2741+40_2741+42dup
ENST00000548169.2:c.2412+40_2412+42dup
NM_001681.3:c.2741+40_2741+42dup NP_001672.1:n.2741+40_2741+42dup
NM_170665.3:c.2741+40_2741+42dup NP_733765.1:n.2741+40_2741+42dup
XM_005253888.1:c.2741+40_2741+42dup XP_005253945.1:n.2741+40_2741+42dup
XM_011538402.1:c.2741+40_2741+42dup XP_011536704.1:n.2741+40_2741+42dup
XR_243009.1:n.2747+40_2747+42dup
XM_005253888.3:c.2741+40_2741+42dup XP_005253945.1:n.2741+40_2741+42dup
XM_011538402.3:c.2741+40_2741+42dup XP_011536704.1:n.2741+40_2741+42dup
XR_002957329.1:n.2747+40_2747+42dup
XR_243009.3:n.2747+40_2747+42dup
NM_170665.4:c.2741+40_2741+42dup MANE Select NP_733765.1:n.2741+40_2741+42dup
NM_001681.4:c.2741+40_2741+42dup NP_001672.1:n.2741+40_2741+42dup