Canonical Allele Identifier: CA2575695026
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42360164_42360168del , CM000677.2:g.42360164_42360168del GRCh38
NC_000015.9:g.42652362_42652366del , CM000677.1:g.42652362_42652366del GRCh37
NC_000015.8:g.40439654_40439658del NCBI36
NG_008660.1:g.17062_17066del

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.309+50_309+54del ENSP00000183936.4:n.309+50_309+54del
ENST00000357568.8:c.309+50_309+54del ENSP00000350181.3:n.309+50_309+54del
ENST00000397163.8:c.309+50_309+54del MANE Select ENSP00000380349.3:n.309+50_309+54del
ENST00000466369.5:n.540+5711_540+5715del
ENST00000483208.5:n.540+5711_540+5715del
ENST00000495723.1:n.540+5711_540+5715del
ENST00000549793.5:n.540+5711_540+5715del
ENST00000318023.11:c.309+50_309+54del ENSP00000326281.8:n.309+50_309+54del
ENST00000349748.7:c.309+50_309+54del ENSP00000183936.4:n.309+50_309+54del
ENST00000357568.7:c.309+50_309+54del ENSP00000350181.3:n.309+50_309+54del
ENST00000397163.7:c.309+50_309+54del ENSP00000380349.3:n.309+50_309+54del
NM_000070.2:c.309+50_309+54del NP_000061.1:n.309+50_309+54del
NM_024344.1:c.309+50_309+54del NP_077320.1:n.309+50_309+54del
NM_173087.1:c.309+50_309+54del NP_775110.1:n.309+50_309+54del
NM_000070.3:c.309+50_309+54del MANE Select NP_000061.1:n.309+50_309+54del
NM_024344.2:c.309+50_309+54del NP_077320.1:n.309+50_309+54del
NM_173087.2:c.309+50_309+54del NP_775110.1:n.309+50_309+54del