Canonical Allele Identifier: CA391999767
Gene: CAPN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1473589
ClinVar RCV Id: RCV001970769
dbSNP Id: rs2141199495

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42401689A>G , CM000677.2:g.42401689A>G GRCh38
NC_000015.9:g.42693887A>G , CM000677.1:g.42693887A>G GRCh37
NC_000015.8:g.40481179A>G NCBI36
NG_008660.1:g.58587A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.1259A>G ENSP00000183936.4:p.Asp420Gly
ENST00000357568.8:c.1403A>G ENSP00000350181.3:p.Asp468Gly
ENST00000397163.8:c.1403A>G MANE Select ENSP00000380349.3:p.Asp468Gly
ENST00000466369.5:n.1912A>G
ENST00000483208.5:n.1634A>G
ENST00000495723.1:n.1634A>G
ENST00000549793.5:n.1634A>G
ENST00000638141.2:n.1274A>G
ENST00000673705.1:c.309+2037A>G ENSP00000501021.1:n.309+2037A>G
ENST00000318023.11:c.1259A>G ENSP00000326281.8:p.Asp420Gly
ENST00000349748.7:c.1259A>G ENSP00000183936.4:p.Asp420Gly
ENST00000357568.7:c.1403A>G ENSP00000350181.3:p.Asp468Gly
ENST00000397163.7:c.1403A>G ENSP00000380349.3:p.Asp468Gly
NM_000070.2:c.1403A>G NP_000061.1:p.Asp468Gly
NM_024344.1:c.1403A>G NP_077320.1:p.Asp468Gly
NM_173087.1:c.1259A>G NP_775110.1:p.Asp420Gly
NM_000070.3:c.1403A>G MANE Select NP_000061.1:p.Asp468Gly
NM_024344.2:c.1403A>G NP_077320.1:p.Asp468Gly
NM_173087.2:c.1259A>G NP_775110.1:p.Asp420Gly