Canonical Allele Identifier: CA2172720440
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42409972C= , CM000677.2:g.42409972C= GRCh38
NC_000015.9:g.42702170C= , CM000677.1:g.42702170C= GRCh37
NC_000015.8:g.40489462C= NCBI36
NG_008660.1:g.66870C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337571.9:c.97C= ENSP00000336840.4:p.Arg33=
ENST00000349748.8:c.1816C= ENSP00000183936.4:p.Arg606=
ENST00000357568.8:c.2074C= ENSP00000350181.3:p.Arg692=
ENST00000397163.8:c.2092C= MANE Select ENSP00000380349.3:p.Arg698=
ENST00000397204.9:c.97C= ENSP00000380387.4:p.Arg33=
ENST00000466222.7:n.357C=
ENST00000466369.5:n.2583C=
ENST00000495723.1:n.2963C=
ENST00000549793.5:n.2305C=
ENST00000562199.2:c.100C= ENSP00000501034.1:p.Arg34=
ENST00000569136.6:c.97C= ENSP00000455254.1:p.Arg33=
ENST00000638141.2:n.1831C=
ENST00000673646.1:c.656C= ENSP00000501007.1:n.656C=
ENST00000673687.1:n.169C=
ENST00000673692.1:c.97C= ENSP00000501138.1:p.Arg33=
ENST00000673705.1:c.487C= ENSP00000501021.1:n.487C=
ENST00000673743.1:c.-6C= ENSP00000500989.1:n.-6C=
ENST00000673750.1:c.97C= ENSP00000501173.1:p.Arg33=
ENST00000673771.1:c.97C= ENSP00000501023.1:p.Arg33=
ENST00000673774.1:n.793C=
ENST00000673839.1:c.97C= ENSP00000501188.1:p.Arg33=
ENST00000673851.1:c.97C= ENSP00000501142.1:p.Arg33=
ENST00000673854.1:n.5514C=
ENST00000673886.1:c.97C= ENSP00000501155.1:p.Arg33=
ENST00000673890.1:c.97C= ENSP00000501293.1:p.Arg33=
ENST00000673893.1:c.16C= ENSP00000500987.1:p.Arg6=
ENST00000673928.1:c.97C= ENSP00000501099.1:p.Arg33=
ENST00000673936.1:c.97C= ENSP00000501189.1:p.Arg33=
ENST00000673939.1:c.97C= ENSP00000501129.1:p.Arg33=
ENST00000673950.1:n.366C=
ENST00000673978.1:c.235C= ENSP00000500976.1:p.Arg79=
ENST00000673987.1:c.97C= ENSP00000501231.1:p.Arg33=
ENST00000674011.1:c.97C= ENSP00000501171.1:p.Arg33=
ENST00000674018.1:c.97C= ENSP00000501271.1:p.Arg33=
ENST00000674027.1:n.152C=
ENST00000674041.1:c.97C= ENSP00000500956.1:p.Arg33=
ENST00000674052.1:c.316C= ENSP00000501057.1:p.Arg106=
ENST00000674093.1:c.97C= ENSP00000501303.1:p.Arg33=
ENST00000674119.1:c.97C= ENSP00000501217.1:p.Arg33=
ENST00000674130.1:n.310C=
ENST00000674135.1:c.274C= ENSP00000501178.1:p.Arg92=
ENST00000674139.1:c.97C= ENSP00000501054.1:p.Arg33=
ENST00000674146.1:c.97C= ENSP00000501175.1:p.Arg33=
ENST00000674149.1:c.97C= ENSP00000501112.1:p.Arg33=
ENST00000318023.11:c.1948C= ENSP00000326281.8:p.Arg650=
ENST00000337571.8:c.97C= ENSP00000336840.4:p.Arg33=
ENST00000349748.7:c.1816C= ENSP00000183936.4:p.Arg606=
ENST00000356316.7:c.97C= ENSP00000348667.4:p.Arg33=
ENST00000357568.7:c.2074C= ENSP00000350181.3:p.Arg692=
ENST00000397163.7:c.2092C= ENSP00000380349.3:p.Arg698=
ENST00000397200.8:c.556C= ENSP00000380384.4:p.Arg186=
ENST00000397204.8:c.97C= ENSP00000380387.4:p.Arg33=
ENST00000466222.6:n.1015C=
ENST00000561817.5:c.97C= ENSP00000456575.1:p.Arg33=
ENST00000562199.1:n.100C=
ENST00000564503.5:c.189C=
ENST00000565274.5:c.304C= ENSP00000457759.1:p.Arg102=
ENST00000565559.5:c.274C= ENSP00000457878.1:p.Arg92=
ENST00000569136.5:c.97C= ENSP00000455254.1:p.Arg33=
ENST00000569827.5:c.424C= ENSP00000454379.1:p.Arg142=
NM_000070.2:c.2092C= NP_000061.1:p.Arg698=
NM_024344.1:c.2074C= NP_077320.1:p.Arg692=
NM_173087.1:c.1816C= NP_775110.1:p.Arg606=
NM_173088.1:c.556C= NP_775111.1:p.Arg186=
NM_173089.1:c.97C= NP_775112.1:p.Arg33=
NM_173090.1:c.97C= NP_775113.1:p.Arg33=
NM_000070.3:c.2092C= MANE Select NP_000061.1:p.Arg698=
NM_024344.2:c.2074C= NP_077320.1:p.Arg692=
NM_173087.2:c.1816C= NP_775110.1:p.Arg606=
NM_173088.2:c.556C= NP_775111.1:p.Arg186=
NM_173089.2:c.97C= NP_775112.1:p.Arg33=
NM_173090.2:c.97C= NP_775113.1:p.Arg33=