Canonical Allele Identifier: CA391999881
Gene: CAPN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42401741G>C , CM000677.2:g.42401741G>C GRCh38
NC_000015.9:g.42693939G>C , CM000677.1:g.42693939G>C GRCh37
NC_000015.8:g.40481231G>C NCBI36
NG_008660.1:g.58639G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.1311G>C ENSP00000183936.4:p.Met437Ile
ENST00000357568.8:c.1455G>C ENSP00000350181.3:p.Met485Ile
ENST00000397163.8:c.1455G>C MANE Select ENSP00000380349.3:p.Met485Ile
ENST00000466369.5:n.1964G>C
ENST00000483208.5:n.1686G>C
ENST00000495723.1:n.1686G>C
ENST00000549793.5:n.1686G>C
ENST00000638141.2:n.1326G>C
ENST00000673705.1:c.309+2089G>C ENSP00000501021.1:n.309+2089G>C
ENST00000318023.11:c.1311G>C ENSP00000326281.8:p.Met437Ile
ENST00000349748.7:c.1311G>C ENSP00000183936.4:p.Met437Ile
ENST00000357568.7:c.1455G>C ENSP00000350181.3:p.Met485Ile
ENST00000397163.7:c.1455G>C ENSP00000380349.3:p.Met485Ile
NM_000070.2:c.1455G>C NP_000061.1:p.Met485Ile
NM_024344.1:c.1455G>C NP_077320.1:p.Met485Ile
NM_173087.1:c.1311G>C NP_775110.1:p.Met437Ile
NM_000070.3:c.1455G>C MANE Select NP_000061.1:p.Met485Ile
NM_024344.2:c.1455G>C NP_077320.1:p.Met485Ile
NM_173087.2:c.1311G>C NP_775110.1:p.Met437Ile