Canonical Allele Identifier: CA2620870205
Gene: ATP2A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110343575_110343576insATC , CM000674.2:g.110343575_110343576insATC GRCh38
NC_000012.11:g.110781380_110781381insATC , CM000674.1:g.110781380_110781381insATC GRCh37
NC_000012.10:g.109265763_109265764insATC NCBI36
NG_007097.2:g.66949_66950insATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.2521+141_2521+142insATC MANE Select ENSP00000440045.2:n.2521+141_2521+142insATC
ENST00000308664.10:c.2521+141_2521+142insATC ENSP00000311186.6:n.2521+141_2521+142insATC
ENST00000377685.9:c.*2361+141_*2361+142insATC ENSP00000366913.4:n.*2361+141_*2361+142insATC
ENST00000539276.6:c.2521+141_2521+142insATC ENSP00000440045.2:n.2521+141_2521+142insATC
ENST00000547792.1:n.179+141_179+142insATC
ENST00000548169.2:c.2192+141_2192+142insATC
NM_001681.3:c.2521+141_2521+142insATC NP_001672.1:n.2521+141_2521+142insATC
NM_170665.3:c.2521+141_2521+142insATC NP_733765.1:n.2521+141_2521+142insATC
XM_005253888.1:c.2521+141_2521+142insATC XP_005253945.1:n.2521+141_2521+142insATC
XM_011538402.1:c.2521+141_2521+142insATC XP_011536704.1:n.2521+141_2521+142insATC
XM_011538403.1:c.2521+141_2521+142insATC XP_011536705.1:n.2521+141_2521+142insATC
XR_243009.1:n.2527+141_2527+142insATC
XM_005253888.3:c.2521+141_2521+142insATC XP_005253945.1:n.2521+141_2521+142insATC
XM_011538402.3:c.2521+141_2521+142insATC XP_011536704.1:n.2521+141_2521+142insATC
XR_002957329.1:n.2527+141_2527+142insATC
XR_243009.3:n.2527+141_2527+142insATC
NM_170665.4:c.2521+141_2521+142insATC MANE Select NP_733765.1:n.2521+141_2521+142insATC
NM_001681.4:c.2521+141_2521+142insATC NP_001672.1:n.2521+141_2521+142insATC