Canonical Allele Identifier: CA2172721146
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42411297T= , CM000677.2:g.42411297T= GRCh38
NC_000015.9:g.42703495T= , CM000677.1:g.42703495T= GRCh37
NC_000015.8:g.40490787T= NCBI36
NG_008660.1:g.68195T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337571.9:c.396T= ENSP00000336840.4:p.His132=
ENST00000349748.8:c.2115T= ENSP00000183936.4:p.His705=
ENST00000357568.8:c.2373T= ENSP00000350181.3:p.His791=
ENST00000397163.8:c.2391T= MANE Select ENSP00000380349.3:p.His797=
ENST00000397204.9:c.396T= ENSP00000380387.4:p.His132=
ENST00000466222.7:n.762T=
ENST00000466369.5:n.2882T=
ENST00000495723.1:n.3262T=
ENST00000549793.5:n.2604T=
ENST00000562199.2:c.395T= ENSP00000501034.1:n.395T=
ENST00000567817.6:c.180T= ENSP00000456514.2:p.His60=
ENST00000568153.2:c.257T=
ENST00000569136.6:c.396T= ENSP00000455254.1:p.His132=
ENST00000638141.2:n.2130T=
ENST00000673646.1:c.955T= ENSP00000501007.1:n.955T=
ENST00000673684.1:n.373T=
ENST00000673692.1:c.396T= ENSP00000501138.1:p.His132=
ENST00000673705.1:c.1220T= ENSP00000501021.1:n.1220T=
ENST00000673743.1:c.294T= ENSP00000500989.1:p.His98=
ENST00000673750.1:c.396T= ENSP00000501173.1:p.His132=
ENST00000673771.1:c.396T= ENSP00000501023.1:p.His132=
ENST00000673774.1:n.1524T=
ENST00000673839.1:c.396T= ENSP00000501188.1:p.His132=
ENST00000673851.1:c.396T= ENSP00000501142.1:p.His132=
ENST00000673854.1:n.5813T=
ENST00000673886.1:c.396T= ENSP00000501155.1:p.His132=
ENST00000673890.1:c.396T= ENSP00000501293.1:p.His132=
ENST00000673928.1:c.396T= ENSP00000501099.1:p.His132=
ENST00000673936.1:c.396T= ENSP00000501189.1:p.His132=
ENST00000673939.1:c.*111T= ENSP00000501129.1:n.*111T=
ENST00000673950.1:n.665T=
ENST00000673978.1:c.534T= ENSP00000500976.1:p.His178=
ENST00000673987.1:c.*111T= ENSP00000501231.1:n.*111T=
ENST00000674011.1:c.*185T= ENSP00000501171.1:n.*185T=
ENST00000674018.1:c.396T= ENSP00000501271.1:p.His132=
ENST00000674027.1:n.542T=
ENST00000674041.1:c.396T= ENSP00000500956.1:p.His132=
ENST00000674052.1:c.615T= ENSP00000501057.1:p.His205=
ENST00000674093.1:c.396T= ENSP00000501303.1:p.His132=
ENST00000674119.1:c.396T= ENSP00000501217.1:p.His132=
ENST00000674135.1:c.573T= ENSP00000501178.1:p.His191=
ENST00000674139.1:c.396T= ENSP00000501054.1:p.His132=
ENST00000674146.1:c.396T= ENSP00000501175.1:p.His132=
ENST00000674149.1:c.396T= ENSP00000501112.1:p.His132=
ENST00000318023.11:c.2247T= ENSP00000326281.8:p.His749=
ENST00000337571.8:c.396T= ENSP00000336840.4:p.His132=
ENST00000349748.7:c.2115T= ENSP00000183936.4:p.His705=
ENST00000356316.7:c.396T= ENSP00000348667.4:p.His132=
ENST00000357568.7:c.2373T= ENSP00000350181.3:p.His791=
ENST00000397163.7:c.2391T= ENSP00000380349.3:p.His797=
ENST00000397200.8:c.855T= ENSP00000380384.4:p.His285=
ENST00000397204.8:c.396T= ENSP00000380387.4:p.His132=
ENST00000466222.6:n.1314T=
ENST00000561817.5:c.396T= ENSP00000456575.1:p.His132=
ENST00000564503.5:c.434T=
ENST00000565274.5:c.569T= ENSP00000457759.1:n.569T=
ENST00000567817.5:c.207T= ENSP00000456514.1:p.His69=
ENST00000568153.1:c.128T=
ENST00000569136.5:c.396T= ENSP00000455254.1:p.His132=
ENST00000569827.5:c.723T= ENSP00000454379.1:p.His241=
NM_000070.2:c.2391T= NP_000061.1:p.His797=
NM_024344.1:c.2373T= NP_077320.1:p.His791=
NM_173087.1:c.2115T= NP_775110.1:p.His705=
NM_173088.1:c.855T= NP_775111.1:p.His285=
NM_173089.1:c.396T= NP_775112.1:p.His132=
NM_173090.1:c.396T= NP_775113.1:p.His132=
NM_000070.3:c.2391T= MANE Select NP_000061.1:p.His797=
NM_024344.2:c.2373T= NP_077320.1:p.His791=
NM_173087.2:c.2115T= NP_775110.1:p.His705=
NM_173088.2:c.855T= NP_775111.1:p.His285=
NM_173089.2:c.396T= NP_775112.1:p.His132=
NM_173090.2:c.396T= NP_775113.1:p.His132=