Canonical Allele Identifier: CA2172697509
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42360208_42360209delinsTG , CM000677.2:g.42360208_42360209delinsTG GRCh38
NC_000015.9:g.42652406_42652407delinsTG , CM000677.1:g.42652406_42652407delinsTG GRCh37
NC_000015.8:g.40439698_40439699delinsTG NCBI36
NG_008660.1:g.17106_17107delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.309+94_309+95delinsTG ENSP00000183936.4:n.309+94_309+95delinsTG
ENST00000357568.8:c.309+94_309+95delinsTG ENSP00000350181.3:n.309+94_309+95delinsTG
ENST00000397163.8:c.309+94_309+95delinsTG MANE Select ENSP00000380349.3:n.309+94_309+95delinsTG
ENST00000466369.5:n.540+5755_540+5756delinsTG
ENST00000483208.5:n.540+5755_540+5756delinsTG
ENST00000495723.1:n.540+5755_540+5756delinsTG
ENST00000549793.5:n.540+5755_540+5756delinsTG
ENST00000318023.11:c.309+94_309+95delinsTG ENSP00000326281.8:n.309+94_309+95delinsTG
ENST00000349748.7:c.309+94_309+95delinsTG ENSP00000183936.4:n.309+94_309+95delinsTG
ENST00000357568.7:c.309+94_309+95delinsTG ENSP00000350181.3:n.309+94_309+95delinsTG
ENST00000397163.7:c.309+94_309+95delinsTG ENSP00000380349.3:n.309+94_309+95delinsTG
NM_000070.2:c.309+94_309+95delinsTG NP_000061.1:n.309+94_309+95delinsTG
NM_024344.1:c.309+94_309+95delinsTG NP_077320.1:n.309+94_309+95delinsTG
NM_173087.1:c.309+94_309+95delinsTG NP_775110.1:n.309+94_309+95delinsTG
NM_000070.3:c.309+94_309+95delinsTG MANE Select NP_000061.1:n.309+94_309+95delinsTG
NM_024344.2:c.309+94_309+95delinsTG NP_077320.1:n.309+94_309+95delinsTG
NM_173087.2:c.309+94_309+95delinsTG NP_775110.1:n.309+94_309+95delinsTG