Canonical Allele Identifier: CA2172712031
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42392596T= , CM000677.2:g.42392596T= GRCh38
NC_000015.9:g.42684794T= , CM000677.1:g.42684794T= GRCh37
NC_000015.8:g.40472086T= NCBI36
NG_008660.1:g.49494T=

Transcript Alleles

HGVS Amino-acid change
ENST00000349748.8:c.802-43T= ENSP00000183936.4:n.802-43T=
ENST00000357568.8:c.946-43T= ENSP00000350181.3:n.946-43T=
ENST00000397163.8:c.946-43T= MANE Select ENSP00000380349.3:n.946-43T=
ENST00000466369.5:n.1455-43T=
ENST00000483208.5:n.1177-43T=
ENST00000495723.1:n.1177-43T=
ENST00000549793.5:n.1177-43T=
ENST00000638141.2:n.817-43T=
ENST00000673705.1:c.71-4204T= ENSP00000501021.1:n.71-4204T=
ENST00000318023.11:c.802-43T= ENSP00000326281.8:n.802-43T=
ENST00000349748.7:c.802-43T= ENSP00000183936.4:n.802-43T=
ENST00000357568.7:c.946-43T= ENSP00000350181.3:n.946-43T=
ENST00000397163.7:c.946-43T= ENSP00000380349.3:n.946-43T=
NM_000070.2:c.946-43T= NP_000061.1:n.946-43T=
NM_024344.1:c.946-43T= NP_077320.1:n.946-43T=
NM_173087.1:c.802-43T= NP_775110.1:n.802-43T=
NM_000070.3:c.946-43T= MANE Select NP_000061.1:n.946-43T=
NM_024344.2:c.946-43T= NP_077320.1:n.946-43T=
NM_173087.2:c.802-43T= NP_775110.1:n.802-43T=