Canonical Allele Identifier: CA2172718951
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42401659C= , CM000677.2:g.42401659C= GRCh38
NC_000015.9:g.42693857C= , CM000677.1:g.42693857C= GRCh37
NC_000015.8:g.40481149C= NCBI36
NG_008660.1:g.58557C=

Transcript Alleles

HGVS Amino-acid change
ENST00000349748.8:c.1229C= ENSP00000183936.4:p.Pro410=
ENST00000357568.8:c.1373C= ENSP00000350181.3:p.Pro458=
ENST00000397163.8:c.1373C= MANE Select ENSP00000380349.3:p.Pro458=
ENST00000466369.5:n.1882C=
ENST00000483208.5:n.1604C=
ENST00000495723.1:n.1604C=
ENST00000549793.5:n.1604C=
ENST00000638141.2:n.1244C=
ENST00000673705.1:c.309+2007C= ENSP00000501021.1:n.309+2007C=
ENST00000318023.11:c.1229C= ENSP00000326281.8:p.Pro410=
ENST00000349748.7:c.1229C= ENSP00000183936.4:p.Pro410=
ENST00000357568.7:c.1373C= ENSP00000350181.3:p.Pro458=
ENST00000397163.7:c.1373C= ENSP00000380349.3:p.Pro458=
NM_000070.2:c.1373C= NP_000061.1:p.Pro458=
NM_024344.1:c.1373C= NP_077320.1:p.Pro458=
NM_173087.1:c.1229C= NP_775110.1:p.Pro410=
NM_000070.3:c.1373C= MANE Select NP_000061.1:p.Pro458=
NM_024344.2:c.1373C= NP_077320.1:p.Pro458=
NM_173087.2:c.1229C= NP_775110.1:p.Pro410=