Canonical Allele Identifier: CA2172720441
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42409973G= , CM000677.2:g.42409973G= GRCh38
NC_000015.9:g.42702171G= , CM000677.1:g.42702171G= GRCh37
NC_000015.8:g.40489463G= NCBI36
NG_008660.1:g.66871G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337571.9:c.98G= ENSP00000336840.4:p.Arg33=
ENST00000349748.8:c.1817G= ENSP00000183936.4:p.Arg606=
ENST00000357568.8:c.2075G= ENSP00000350181.3:p.Arg692=
ENST00000397163.8:c.2093G= MANE Select ENSP00000380349.3:p.Arg698=
ENST00000397204.9:c.98G= ENSP00000380387.4:p.Arg33=
ENST00000466222.7:n.358G=
ENST00000466369.5:n.2584G=
ENST00000495723.1:n.2964G=
ENST00000549793.5:n.2306G=
ENST00000562199.2:c.101G= ENSP00000501034.1:p.Arg34=
ENST00000569136.6:c.98G= ENSP00000455254.1:p.Arg33=
ENST00000638141.2:n.1832G=
ENST00000673646.1:c.657G= ENSP00000501007.1:n.657G=
ENST00000673687.1:n.170G=
ENST00000673692.1:c.98G= ENSP00000501138.1:p.Arg33=
ENST00000673705.1:c.488G= ENSP00000501021.1:n.488G=
ENST00000673743.1:c.-5G= ENSP00000500989.1:n.-5G=
ENST00000673750.1:c.98G= ENSP00000501173.1:p.Arg33=
ENST00000673771.1:c.98G= ENSP00000501023.1:p.Arg33=
ENST00000673774.1:n.794G=
ENST00000673839.1:c.98G= ENSP00000501188.1:p.Arg33=
ENST00000673851.1:c.98G= ENSP00000501142.1:p.Arg33=
ENST00000673854.1:n.5515G=
ENST00000673886.1:c.98G= ENSP00000501155.1:p.Arg33=
ENST00000673890.1:c.98G= ENSP00000501293.1:p.Arg33=
ENST00000673893.1:c.17G= ENSP00000500987.1:p.Arg6=
ENST00000673928.1:c.98G= ENSP00000501099.1:p.Arg33=
ENST00000673936.1:c.98G= ENSP00000501189.1:p.Arg33=
ENST00000673939.1:c.98G= ENSP00000501129.1:p.Arg33=
ENST00000673950.1:n.367G=
ENST00000673978.1:c.236G= ENSP00000500976.1:p.Arg79=
ENST00000673987.1:c.98G= ENSP00000501231.1:p.Arg33=
ENST00000674011.1:c.98G= ENSP00000501171.1:p.Arg33=
ENST00000674018.1:c.98G= ENSP00000501271.1:p.Arg33=
ENST00000674027.1:n.153G=
ENST00000674041.1:c.98G= ENSP00000500956.1:p.Arg33=
ENST00000674052.1:c.317G= ENSP00000501057.1:p.Arg106=
ENST00000674093.1:c.98G= ENSP00000501303.1:p.Arg33=
ENST00000674119.1:c.98G= ENSP00000501217.1:p.Arg33=
ENST00000674130.1:n.311G=
ENST00000674135.1:c.275G= ENSP00000501178.1:p.Arg92=
ENST00000674139.1:c.98G= ENSP00000501054.1:p.Arg33=
ENST00000674146.1:c.98G= ENSP00000501175.1:p.Arg33=
ENST00000674149.1:c.98G= ENSP00000501112.1:p.Arg33=
ENST00000318023.11:c.1949G= ENSP00000326281.8:p.Arg650=
ENST00000337571.8:c.98G= ENSP00000336840.4:p.Arg33=
ENST00000349748.7:c.1817G= ENSP00000183936.4:p.Arg606=
ENST00000356316.7:c.98G= ENSP00000348667.4:p.Arg33=
ENST00000357568.7:c.2075G= ENSP00000350181.3:p.Arg692=
ENST00000397163.7:c.2093G= ENSP00000380349.3:p.Arg698=
ENST00000397200.8:c.557G= ENSP00000380384.4:p.Arg186=
ENST00000397204.8:c.98G= ENSP00000380387.4:p.Arg33=
ENST00000466222.6:n.1016G=
ENST00000561817.5:c.98G= ENSP00000456575.1:p.Arg33=
ENST00000562199.1:n.101G=
ENST00000564503.5:c.190G=
ENST00000565274.5:c.305G= ENSP00000457759.1:p.Arg102=
ENST00000565559.5:c.275G= ENSP00000457878.1:p.Arg92=
ENST00000569136.5:c.98G= ENSP00000455254.1:p.Arg33=
ENST00000569827.5:c.425G= ENSP00000454379.1:p.Arg142=
NM_000070.2:c.2093G= NP_000061.1:p.Arg698=
NM_024344.1:c.2075G= NP_077320.1:p.Arg692=
NM_173087.1:c.1817G= NP_775110.1:p.Arg606=
NM_173088.1:c.557G= NP_775111.1:p.Arg186=
NM_173089.1:c.98G= NP_775112.1:p.Arg33=
NM_173090.1:c.98G= NP_775113.1:p.Arg33=
NM_000070.3:c.2093G= MANE Select NP_000061.1:p.Arg698=
NM_024344.2:c.2075G= NP_077320.1:p.Arg692=
NM_173087.2:c.1817G= NP_775110.1:p.Arg606=
NM_173088.2:c.557G= NP_775111.1:p.Arg186=
NM_173089.2:c.98G= NP_775112.1:p.Arg33=
NM_173090.2:c.98G= NP_775113.1:p.Arg33=