Canonical Allele Identifier: CA10606714
Gene: CAPN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 290265
dbSNP Id: rs886044405

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42388989A>C , CM000677.2:g.42388989A>C GRCh38
NC_000015.9:g.42681187A>C , CM000677.1:g.42681187A>C GRCh37
NC_000015.8:g.40468479A>C NCBI36
NG_008660.1:g.45887A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.694A>C ENSP00000183936.4:p.Thr232Pro
ENST00000357568.8:c.694A>C ENSP00000350181.3:p.Thr232Pro
ENST00000397163.8:c.694A>C MANE Select ENSP00000380349.3:p.Thr232Pro
ENST00000466369.5:n.1203A>C
ENST00000483208.5:n.925A>C
ENST00000495723.1:n.925A>C
ENST00000549793.5:n.925A>C
ENST00000638141.2:n.709A>C
ENST00000673705.1:c.70+4437A>C ENSP00000501021.1:n.70+4437A>C
ENST00000318023.11:c.694A>C ENSP00000326281.8:p.Thr232Pro
ENST00000349748.7:c.694A>C ENSP00000183936.4:p.Thr232Pro
ENST00000357568.7:c.694A>C ENSP00000350181.3:p.Thr232Pro
ENST00000397163.7:c.694A>C ENSP00000380349.3:p.Thr232Pro
NM_000070.2:c.694A>C NP_000061.1:p.Thr232Pro
NM_024344.1:c.694A>C NP_077320.1:p.Thr232Pro
NM_173087.1:c.694A>C NP_775110.1:p.Thr232Pro
NM_000070.3:c.694A>C MANE Select NP_000061.1:p.Thr232Pro
NM_024344.2:c.694A>C NP_077320.1:p.Thr232Pro
NM_173087.2:c.694A>C NP_775110.1:p.Thr232Pro