Canonical Allele Identifier: CA617605404
Gene: CAPN3 HGNC NCBI

Linked Data

dbSNP Id: rs1231638797

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42392619C>T , CM000677.2:g.42392619C>T GRCh38
NC_000015.9:g.42684817C>T , CM000677.1:g.42684817C>T GRCh37
NC_000015.8:g.40472109C>T NCBI36
NG_008660.1:g.49517C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000349748.8:c.802-20C>T ENSP00000183936.4:n.802-20C>T
ENST00000357568.8:c.946-20C>T ENSP00000350181.3:n.946-20C>T
ENST00000397163.8:c.946-20C>T MANE Select ENSP00000380349.3:n.946-20C>T
ENST00000466369.5:n.1455-20C>T
ENST00000483208.5:n.1177-20C>T
ENST00000495723.1:n.1177-20C>T
ENST00000549793.5:n.1177-20C>T
ENST00000638141.2:n.817-20C>T
ENST00000673705.1:c.71-4181C>T ENSP00000501021.1:n.71-4181C>T
ENST00000318023.11:c.802-20C>T ENSP00000326281.8:n.802-20C>T
ENST00000349748.7:c.802-20C>T ENSP00000183936.4:n.802-20C>T
ENST00000357568.7:c.946-20C>T ENSP00000350181.3:n.946-20C>T
ENST00000397163.7:c.946-20C>T ENSP00000380349.3:n.946-20C>T
NM_000070.2:c.946-20C>T NP_000061.1:n.946-20C>T
NM_024344.1:c.946-20C>T NP_077320.1:n.946-20C>T
NM_173087.1:c.802-20C>T NP_775110.1:n.802-20C>T
NM_000070.3:c.946-20C>T MANE Select NP_000061.1:n.946-20C>T
NM_024344.2:c.946-20C>T NP_077320.1:n.946-20C>T
NM_173087.2:c.802-20C>T NP_775110.1:n.802-20C>T