Canonical Allele Identifier: CA2172720982
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42410958G= , CM000677.2:g.42410958G= GRCh38
NC_000015.9:g.42703156G= , CM000677.1:g.42703156G= GRCh37
NC_000015.8:g.40490448G= NCBI36
NG_008660.1:g.67856G=

Transcript Alleles

HGVS Amino-acid change
ENST00000337571.9:c.343G= ENSP00000336840.4:p.Asp115=
ENST00000349748.8:c.2062G= ENSP00000183936.4:p.Asp688=
ENST00000357568.8:c.2320G= ENSP00000350181.3:p.Asp774=
ENST00000397163.8:c.2338G= MANE Select ENSP00000380349.3:p.Asp780=
ENST00000397204.9:c.343G= ENSP00000380387.4:p.Asp115=
ENST00000466222.7:n.751+32G=
ENST00000466369.5:n.2829G=
ENST00000495723.1:n.3209G=
ENST00000549793.5:n.2551G=
ENST00000562199.2:c.342G= ENSP00000501034.1:n.342G=
ENST00000567817.6:c.127G= ENSP00000456514.2:p.Asp43=
ENST00000568153.2:c.204G=
ENST00000569136.6:c.343G= ENSP00000455254.1:p.Asp115=
ENST00000638141.2:n.2077G=
ENST00000673646.1:c.902G= ENSP00000501007.1:n.902G=
ENST00000673684.1:n.320G=
ENST00000673692.1:c.343G= ENSP00000501138.1:p.Asp115=
ENST00000673705.1:c.881G= ENSP00000501021.1:n.881G=
ENST00000673743.1:c.241G= ENSP00000500989.1:p.Asp81=
ENST00000673750.1:c.343G= ENSP00000501173.1:p.Asp115=
ENST00000673771.1:c.343G= ENSP00000501023.1:p.Asp115=
ENST00000673774.1:n.1471G=
ENST00000673839.1:c.343G= ENSP00000501188.1:p.Asp115=
ENST00000673851.1:c.343G= ENSP00000501142.1:p.Asp115=
ENST00000673854.1:n.5760G=
ENST00000673886.1:c.343G= ENSP00000501155.1:p.Asp115=
ENST00000673890.1:c.343G= ENSP00000501293.1:p.Asp115=
ENST00000673928.1:c.343G= ENSP00000501099.1:p.Asp115=
ENST00000673936.1:c.343G= ENSP00000501189.1:p.Asp115=
ENST00000673939.1:c.*100+32G= ENSP00000501129.1:n.*100+32G=
ENST00000673950.1:n.612G=
ENST00000673978.1:c.481G= ENSP00000500976.1:p.Asp161=
ENST00000673987.1:c.*100+32G= ENSP00000501231.1:n.*100+32G=
ENST00000674011.1:c.*132G= ENSP00000501171.1:n.*132G=
ENST00000674018.1:c.343G= ENSP00000501271.1:p.Asp115=
ENST00000674027.1:n.489G=
ENST00000674041.1:c.343G= ENSP00000500956.1:p.Asp115=
ENST00000674052.1:c.562G= ENSP00000501057.1:p.Asp188=
ENST00000674093.1:c.343G= ENSP00000501303.1:p.Asp115=
ENST00000674119.1:c.343G= ENSP00000501217.1:p.Asp115=
ENST00000674135.1:c.520G= ENSP00000501178.1:p.Asp174=
ENST00000674139.1:c.343G= ENSP00000501054.1:p.Asp115=
ENST00000674146.1:c.343G= ENSP00000501175.1:p.Asp115=
ENST00000674149.1:c.343G= ENSP00000501112.1:p.Asp115=
ENST00000318023.11:c.2194G= ENSP00000326281.8:p.Asp732=
ENST00000337571.8:c.343G= ENSP00000336840.4:p.Asp115=
ENST00000349748.7:c.2062G= ENSP00000183936.4:p.Asp688=
ENST00000356316.7:c.343G= ENSP00000348667.4:p.Asp115=
ENST00000357568.7:c.2320G= ENSP00000350181.3:p.Asp774=
ENST00000397163.7:c.2338G= ENSP00000380349.3:p.Asp780=
ENST00000397200.8:c.802G= ENSP00000380384.4:p.Asp268=
ENST00000397204.8:c.343G= ENSP00000380387.4:p.Asp115=
ENST00000466222.6:n.1261G=
ENST00000561817.5:c.343G= ENSP00000456575.1:p.Asp115=
ENST00000562199.1:n.342G=
ENST00000564503.5:c.381G=
ENST00000565274.5:c.516G= ENSP00000457759.1:n.516G=
ENST00000567817.5:c.154G= ENSP00000456514.1:p.Asp52=
ENST00000568153.1:c.75G=
ENST00000569136.5:c.343G= ENSP00000455254.1:p.Asp115=
ENST00000569827.5:c.670G= ENSP00000454379.1:p.Asp224=
NM_000070.2:c.2338G= NP_000061.1:p.Asp780=
NM_024344.1:c.2320G= NP_077320.1:p.Asp774=
NM_173087.1:c.2062G= NP_775110.1:p.Asp688=
NM_173088.1:c.802G= NP_775111.1:p.Asp268=
NM_173089.1:c.343G= NP_775112.1:p.Asp115=
NM_173090.1:c.343G= NP_775113.1:p.Asp115=
NM_000070.3:c.2338G= MANE Select NP_000061.1:p.Asp780=
NM_024344.2:c.2320G= NP_077320.1:p.Asp774=
NM_173087.2:c.2062G= NP_775110.1:p.Asp688=
NM_173088.2:c.802G= NP_775111.1:p.Asp268=
NM_173089.2:c.343G= NP_775112.1:p.Asp115=
NM_173090.2:c.343G= NP_775113.1:p.Asp115=