Canonical Allele Identifier: CA386677229
Gene: ATP2A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110345253A>C , CM000674.2:g.110345253A>C GRCh38
NC_000012.11:g.110783058A>C , CM000674.1:g.110783058A>C GRCh37
NC_000012.10:g.109267441A>C NCBI36
NG_007097.2:g.68627A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.2612A>C MANE Select ENSP00000440045.2:p.His871Pro
ENST00000308664.10:c.2612A>C ENSP00000311186.6:p.His871Pro
ENST00000377685.9:c.*2452A>C ENSP00000366913.4:n.*2452A>C
ENST00000539276.6:c.2612A>C ENSP00000440045.2:p.His871Pro
ENST00000548169.2:c.2283A>C
NM_001681.3:c.2612A>C NP_001672.1:p.His871Pro
NM_170665.3:c.2612A>C NP_733765.1:p.His871Pro
XM_005253888.1:c.2612A>C XP_005253945.1:p.His871Pro
XM_011538402.1:c.2612A>C XP_011536704.1:p.His871Pro
XR_243009.1:n.2618A>C
XM_005253888.3:c.2612A>C XP_005253945.1:p.His871Pro
XM_011538402.3:c.2612A>C XP_011536704.1:p.His871Pro
XR_002957329.1:n.2618A>C
XR_243009.3:n.2618A>C
NM_170665.4:c.2612A>C MANE Select NP_733765.1:p.His871Pro
NM_001681.4:c.2612A>C NP_001672.1:p.His871Pro