Canonical Allele Identifier: CA347587
Gene: CAPN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 217150
dbSNP Id: rs863224957

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42401751C>T , CM000677.2:g.42401751C>T GRCh38
NC_000015.9:g.42693949C>T , CM000677.1:g.42693949C>T GRCh37
NC_000015.8:g.40481241C>T NCBI36
NG_008660.1:g.58649C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.1321C>T ENSP00000183936.4:p.Arg441Trp
ENST00000357568.8:c.1465C>T ENSP00000350181.3:p.Arg489Trp
ENST00000397163.8:c.1465C>T MANE Select ENSP00000380349.3:p.Arg489Trp
ENST00000466369.5:n.1974C>T
ENST00000483208.5:n.1696C>T
ENST00000495723.1:n.1696C>T
ENST00000549793.5:n.1696C>T
ENST00000638141.2:n.1336C>T
ENST00000673705.1:c.309+2099C>T ENSP00000501021.1:n.309+2099C>T
ENST00000318023.11:c.1321C>T ENSP00000326281.8:p.Arg441Trp
ENST00000349748.7:c.1321C>T ENSP00000183936.4:p.Arg441Trp
ENST00000357568.7:c.1465C>T ENSP00000350181.3:p.Arg489Trp
ENST00000397163.7:c.1465C>T ENSP00000380349.3:p.Arg489Trp
NM_000070.2:c.1465C>T NP_000061.1:p.Arg489Trp
NM_024344.1:c.1465C>T NP_077320.1:p.Arg489Trp
NM_173087.1:c.1321C>T NP_775110.1:p.Arg441Trp
NM_000070.3:c.1465C>T MANE Select NP_000061.1:p.Arg489Trp
NM_024344.2:c.1465C>T NP_077320.1:p.Arg489Trp
NM_173087.2:c.1321C>T NP_775110.1:p.Arg441Trp