Canonical Allele Identifier: CA489885795
Gene: CAPN3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.42702175C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42409977C>T , CM000677.2:g.42409977C>T GRCh38
NC_000015.9:g.42702175C>T , CM000677.1:g.42702175C>T GRCh37
NC_000015.8:g.40489467C>T NCBI36
NG_008660.1:g.66875C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000337571.9:c.102C>T ENSP00000336840.4:p.Ser34=
ENST00000349748.8:c.1821C>T ENSP00000183936.4:p.Ser607=
ENST00000357568.8:c.2079C>T ENSP00000350181.3:p.Ser693=
ENST00000397163.8:c.2097C>T MANE Select ENSP00000380349.3:p.Ser699=
ENST00000397204.9:c.102C>T ENSP00000380387.4:p.Ser34=
ENST00000466222.7:n.362C>T
ENST00000466369.5:n.2588C>T
ENST00000495723.1:n.2968C>T
ENST00000549793.5:n.2310C>T
ENST00000562199.2:c.105C>T ENSP00000501034.1:p.Ser35=
ENST00000569136.6:c.102C>T ENSP00000455254.1:p.Ser34=
ENST00000638141.2:n.1836C>T
ENST00000673646.1:c.661C>T ENSP00000501007.1:n.661C>T
ENST00000673687.1:n.174C>T
ENST00000673692.1:c.102C>T ENSP00000501138.1:p.Ser34=
ENST00000673705.1:c.492C>T ENSP00000501021.1:n.492C>T
ENST00000673743.1:c.-1C>T ENSP00000500989.1:n.-1C>T
ENST00000673750.1:c.102C>T ENSP00000501173.1:p.Ser34=
ENST00000673771.1:c.102C>T ENSP00000501023.1:p.Ser34=
ENST00000673774.1:n.798C>T
ENST00000673839.1:c.102C>T ENSP00000501188.1:p.Ser34=
ENST00000673851.1:c.102C>T ENSP00000501142.1:p.Ser34=
ENST00000673854.1:n.5519C>T
ENST00000673886.1:c.102C>T ENSP00000501155.1:p.Ser34=
ENST00000673890.1:c.102C>T ENSP00000501293.1:p.Ser34=
ENST00000673893.1:c.21C>T ENSP00000500987.1:p.Ser7=
ENST00000673928.1:c.102C>T ENSP00000501099.1:p.Ser34=
ENST00000673936.1:c.102C>T ENSP00000501189.1:p.Ser34=
ENST00000673939.1:c.102C>T ENSP00000501129.1:p.Ser34=
ENST00000673950.1:n.371C>T
ENST00000673978.1:c.240C>T ENSP00000500976.1:p.Ser80=
ENST00000673987.1:c.102C>T ENSP00000501231.1:p.Ser34=
ENST00000674011.1:c.102C>T ENSP00000501171.1:p.Ser34=
ENST00000674018.1:c.102C>T ENSP00000501271.1:p.Ser34=
ENST00000674027.1:n.157C>T
ENST00000674041.1:c.102C>T ENSP00000500956.1:p.Ser34=
ENST00000674052.1:c.321C>T ENSP00000501057.1:p.Ser107=
ENST00000674093.1:c.102C>T ENSP00000501303.1:p.Ser34=
ENST00000674119.1:c.102C>T ENSP00000501217.1:p.Ser34=
ENST00000674130.1:n.315C>T
ENST00000674135.1:c.279C>T ENSP00000501178.1:p.Ser93=
ENST00000674139.1:c.102C>T ENSP00000501054.1:p.Ser34=
ENST00000674146.1:c.102C>T ENSP00000501175.1:p.Ser34=
ENST00000674149.1:c.102C>T ENSP00000501112.1:p.Ser34=
ENST00000318023.11:c.1953C>T ENSP00000326281.8:p.Ser651=
ENST00000337571.8:c.102C>T ENSP00000336840.4:p.Ser34=
ENST00000349748.7:c.1821C>T ENSP00000183936.4:p.Ser607=
ENST00000356316.7:c.102C>T ENSP00000348667.4:p.Ser34=
ENST00000357568.7:c.2079C>T ENSP00000350181.3:p.Ser693=
ENST00000397163.7:c.2097C>T ENSP00000380349.3:p.Ser699=
ENST00000397200.8:c.561C>T ENSP00000380384.4:p.Ser187=
ENST00000397204.8:c.102C>T ENSP00000380387.4:p.Ser34=
ENST00000466222.6:n.1020C>T
ENST00000561817.5:c.102C>T ENSP00000456575.1:p.Ser34=
ENST00000562199.1:n.105C>T
ENST00000564503.5:c.194C>T
ENST00000565274.5:c.309C>T ENSP00000457759.1:p.Ser103=
ENST00000565559.5:c.279C>T ENSP00000457878.1:p.Ser93=
ENST00000569136.5:c.102C>T ENSP00000455254.1:p.Ser34=
ENST00000569827.5:c.429C>T ENSP00000454379.1:p.Ser143=
NM_000070.2:c.2097C>T NP_000061.1:p.Ser699=
NM_024344.1:c.2079C>T NP_077320.1:p.Ser693=
NM_173087.1:c.1821C>T NP_775110.1:p.Ser607=
NM_173088.1:c.561C>T NP_775111.1:p.Ser187=
NM_173089.1:c.102C>T NP_775112.1:p.Ser34=
NM_173090.1:c.102C>T NP_775113.1:p.Ser34=
NM_000070.3:c.2097C>T MANE Select NP_000061.1:p.Ser699=
NM_024344.2:c.2079C>T NP_077320.1:p.Ser693=
NM_173087.2:c.1821C>T NP_775110.1:p.Ser607=
NM_173088.2:c.561C>T NP_775111.1:p.Ser187=
NM_173089.2:c.102C>T NP_775112.1:p.Ser34=
NM_173090.2:c.102C>T NP_775113.1:p.Ser34=