Canonical Allele Identifier: CA2172720432
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42409959A= , CM000677.2:g.42409959A= GRCh38
NC_000015.9:g.42702157A= , CM000677.1:g.42702157A= GRCh37
NC_000015.8:g.40489449A= NCBI36
NG_008660.1:g.66857A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337571.9:c.84A= ENSP00000336840.4:p.Thr28=
ENST00000349748.8:c.1803A= ENSP00000183936.4:p.Thr601=
ENST00000357568.8:c.2061A= ENSP00000350181.3:p.Thr687=
ENST00000397163.8:c.2079A= MANE Select ENSP00000380349.3:p.Thr693=
ENST00000397204.9:c.84A= ENSP00000380387.4:p.Thr28=
ENST00000466222.7:n.344A=
ENST00000466369.5:n.2570A=
ENST00000495723.1:n.2950A=
ENST00000549793.5:n.2292A=
ENST00000562199.2:c.87A= ENSP00000501034.1:p.Thr29=
ENST00000569136.6:c.84A= ENSP00000455254.1:p.Thr28=
ENST00000638141.2:n.1818A=
ENST00000673646.1:c.643A= ENSP00000501007.1:n.643A=
ENST00000673687.1:n.156A=
ENST00000673692.1:c.84A= ENSP00000501138.1:p.Thr28=
ENST00000673705.1:c.474A= ENSP00000501021.1:n.474A=
ENST00000673743.1:c.-19A= ENSP00000500989.1:n.-19A=
ENST00000673750.1:c.84A= ENSP00000501173.1:p.Thr28=
ENST00000673771.1:c.84A= ENSP00000501023.1:p.Thr28=
ENST00000673774.1:n.780A=
ENST00000673839.1:c.84A= ENSP00000501188.1:p.Thr28=
ENST00000673851.1:c.84A= ENSP00000501142.1:p.Thr28=
ENST00000673854.1:n.5501A=
ENST00000673886.1:c.84A= ENSP00000501155.1:p.Thr28=
ENST00000673890.1:c.84A= ENSP00000501293.1:p.Thr28=
ENST00000673893.1:c.3A= ENSP00000500987.1:p.Thr1=
ENST00000673928.1:c.84A= ENSP00000501099.1:p.Thr28=
ENST00000673936.1:c.84A= ENSP00000501189.1:p.Thr28=
ENST00000673939.1:c.84A= ENSP00000501129.1:p.Thr28=
ENST00000673950.1:n.353A=
ENST00000673978.1:c.222A= ENSP00000500976.1:p.Thr74=
ENST00000673987.1:c.84A= ENSP00000501231.1:p.Thr28=
ENST00000674011.1:c.84A= ENSP00000501171.1:p.Thr28=
ENST00000674018.1:c.84A= ENSP00000501271.1:p.Thr28=
ENST00000674027.1:n.139A=
ENST00000674041.1:c.84A= ENSP00000500956.1:p.Thr28=
ENST00000674052.1:c.303A= ENSP00000501057.1:p.Thr101=
ENST00000674093.1:c.84A= ENSP00000501303.1:p.Thr28=
ENST00000674119.1:c.84A= ENSP00000501217.1:p.Thr28=
ENST00000674130.1:n.297A=
ENST00000674135.1:c.261A= ENSP00000501178.1:p.Thr87=
ENST00000674139.1:c.84A= ENSP00000501054.1:p.Thr28=
ENST00000674146.1:c.84A= ENSP00000501175.1:p.Thr28=
ENST00000674149.1:c.84A= ENSP00000501112.1:p.Thr28=
ENST00000318023.11:c.1935A= ENSP00000326281.8:p.Thr645=
ENST00000337571.8:c.84A= ENSP00000336840.4:p.Thr28=
ENST00000349748.7:c.1803A= ENSP00000183936.4:p.Thr601=
ENST00000356316.7:c.84A= ENSP00000348667.4:p.Thr28=
ENST00000357568.7:c.2061A= ENSP00000350181.3:p.Thr687=
ENST00000397163.7:c.2079A= ENSP00000380349.3:p.Thr693=
ENST00000397200.8:c.543A= ENSP00000380384.4:p.Thr181=
ENST00000397204.8:c.84A= ENSP00000380387.4:p.Thr28=
ENST00000466222.6:n.1002A=
ENST00000561817.5:c.84A= ENSP00000456575.1:p.Thr28=
ENST00000562199.1:n.87A=
ENST00000564503.5:c.176A=
ENST00000565274.5:c.291A= ENSP00000457759.1:p.Thr97=
ENST00000565559.5:c.261A= ENSP00000457878.1:p.Thr87=
ENST00000567071.5:c.559A=
ENST00000569136.5:c.84A= ENSP00000455254.1:p.Thr28=
ENST00000569827.5:c.411A= ENSP00000454379.1:p.Thr137=
NM_000070.2:c.2079A= NP_000061.1:p.Thr693=
NM_024344.1:c.2061A= NP_077320.1:p.Thr687=
NM_173087.1:c.1803A= NP_775110.1:p.Thr601=
NM_173088.1:c.543A= NP_775111.1:p.Thr181=
NM_173089.1:c.84A= NP_775112.1:p.Thr28=
NM_173090.1:c.84A= NP_775113.1:p.Thr28=
NM_000070.3:c.2079A= MANE Select NP_000061.1:p.Thr693=
NM_024344.2:c.2061A= NP_077320.1:p.Thr687=
NM_173087.2:c.1803A= NP_775110.1:p.Thr601=
NM_173088.2:c.543A= NP_775111.1:p.Thr181=
NM_173089.2:c.84A= NP_775112.1:p.Thr28=
NM_173090.2:c.84A= NP_775113.1:p.Thr28=