Canonical Allele Identifier: CA1241849359
Gene: CAPN13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.30806890A= , CM000664.2:g.30806890A= GRCh38
NC_000002.11:g.31029756A= , CM000664.1:g.31029756A= GRCh37
NC_000002.10:g.30883260A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295055.12:c.-33+412T= MANE Select ENSP00000295055.8:n.-33+412T=
ENST00000458085.6:c.-119+412T= ENSP00000416191.2:n.-119+412T=
ENST00000465960.2:n.317+412T=
ENST00000485248.2:c.-119+412T= ENSP00000440723.1:n.-119+412T=
NM_144575.2:c.-33+412T= NP_653176.2:n.-33+412T=
XM_011533159.1:c.-33+412T= XP_011531461.1:n.-33+412T=
XM_011533160.1:c.-119+412T= XP_011531462.1:n.-119+412T=
XM_011533161.1:c.-33+412T= XP_011531463.1:n.-33+412T=
XM_011533162.1:c.-33+412T= XP_011531464.1:n.-33+412T=
XM_011533163.1:c.-33+412T= XP_011531465.1:n.-33+412T=
XR_939741.1:n.145+412T=
XR_939742.1:n.145+412T=
XR_939743.1:n.145+412T=
XM_011533159.3:c.-33+412T= XP_011531461.1:n.-33+412T=
XM_011533160.2:c.-119+412T= XP_011531462.1:n.-119+412T=
XM_011533161.3:c.-33+412T= XP_011531463.1:n.-33+412T=
XM_011533163.3:c.-33+412T= XP_011531465.1:n.-33+412T=
XM_017005264.1:c.-119+412T= XP_016860753.1:n.-119+412T=
XM_017005266.2:c.-33+412T= XP_016860755.1:n.-33+412T=
XR_001739074.1:n.330+412T=
XR_939741.3:n.145+412T=
XR_939742.3:n.145+412T=
XR_939743.3:n.145+412T=
NM_144575.3:c.-33+412T= MANE Select NP_653176.2:n.-33+412T=