Canonical Allele Identifier: CA392001549

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 2098865
• ClinVar RCV Id: RCV003031152
• MyVariant Identifiers: chr15:g.42702174G>A (hg19) ; chr15:g.42409976G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42409976G>A , CM000677.2:g.42409976G>A	GRCh38
NC_000015.9:g.42702174G>A , CM000677.1:g.42702174G>A	GRCh37
NC_000015.8:g.40489466G>A	NCBI36
NG_008660.1:g.66874G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337571.9:c.101G>A	ENSP00000336840.4:p.Ser34Asn
ENST00000349748.8:c.1820G>A	ENSP00000183936.4:p.Ser607Asn
ENST00000357568.8:c.2078G>A	ENSP00000350181.3:p.Ser693Asn
ENST00000397163.8:c.2096G>A MANE Select	ENSP00000380349.3:p.Ser699Asn
ENST00000397204.9:c.101G>A	ENSP00000380387.4:p.Ser34Asn
ENST00000466222.7:n.361G>A
ENST00000466369.5:n.2587G>A
ENST00000495723.1:n.2967G>A
ENST00000549793.5:n.2309G>A
ENST00000562199.2:c.104G>A	ENSP00000501034.1:p.Ser35Asn
ENST00000569136.6:c.101G>A	ENSP00000455254.1:p.Ser34Asn
ENST00000638141.2:n.1835G>A
ENST00000673646.1:c.660G>A	ENSP00000501007.1:n.660G>A
ENST00000673687.1:n.173G>A
ENST00000673692.1:c.101G>A	ENSP00000501138.1:p.Ser34Asn
ENST00000673705.1:c.491G>A	ENSP00000501021.1:n.491G>A
ENST00000673743.1:c.-2G>A	ENSP00000500989.1:n.-2G>A
ENST00000673750.1:c.101G>A	ENSP00000501173.1:p.Ser34Asn
ENST00000673771.1:c.101G>A	ENSP00000501023.1:p.Ser34Asn
ENST00000673774.1:n.797G>A
ENST00000673839.1:c.101G>A	ENSP00000501188.1:p.Ser34Asn
ENST00000673851.1:c.101G>A	ENSP00000501142.1:p.Ser34Asn
ENST00000673854.1:n.5518G>A
ENST00000673886.1:c.101G>A	ENSP00000501155.1:p.Ser34Asn
ENST00000673890.1:c.101G>A	ENSP00000501293.1:p.Ser34Asn
ENST00000673893.1:c.20G>A	ENSP00000500987.1:p.Ser7Asn
ENST00000673928.1:c.101G>A	ENSP00000501099.1:p.Ser34Asn
ENST00000673936.1:c.101G>A	ENSP00000501189.1:p.Ser34Asn
ENST00000673939.1:c.101G>A	ENSP00000501129.1:p.Ser34Asn
ENST00000673950.1:n.370G>A
ENST00000673978.1:c.239G>A	ENSP00000500976.1:p.Ser80Asn
ENST00000673987.1:c.101G>A	ENSP00000501231.1:p.Ser34Asn
ENST00000674011.1:c.101G>A	ENSP00000501171.1:p.Ser34Asn
ENST00000674018.1:c.101G>A	ENSP00000501271.1:p.Ser34Asn
ENST00000674027.1:n.156G>A
ENST00000674041.1:c.101G>A	ENSP00000500956.1:p.Ser34Asn
ENST00000674052.1:c.320G>A	ENSP00000501057.1:p.Ser107Asn
ENST00000674093.1:c.101G>A	ENSP00000501303.1:p.Ser34Asn
ENST00000674119.1:c.101G>A	ENSP00000501217.1:p.Ser34Asn
ENST00000674130.1:n.314G>A
ENST00000674135.1:c.278G>A	ENSP00000501178.1:p.Ser93Asn
ENST00000674139.1:c.101G>A	ENSP00000501054.1:p.Ser34Asn
ENST00000674146.1:c.101G>A	ENSP00000501175.1:p.Ser34Asn
ENST00000674149.1:c.101G>A	ENSP00000501112.1:p.Ser34Asn
ENST00000318023.11:c.1952G>A	ENSP00000326281.8:p.Ser651Asn
ENST00000337571.8:c.101G>A	ENSP00000336840.4:p.Ser34Asn
ENST00000349748.7:c.1820G>A	ENSP00000183936.4:p.Ser607Asn
ENST00000356316.7:c.101G>A	ENSP00000348667.4:p.Ser34Asn
ENST00000357568.7:c.2078G>A	ENSP00000350181.3:p.Ser693Asn
ENST00000397163.7:c.2096G>A	ENSP00000380349.3:p.Ser699Asn
ENST00000397200.8:c.560G>A	ENSP00000380384.4:p.Ser187Asn
ENST00000397204.8:c.101G>A	ENSP00000380387.4:p.Ser34Asn
ENST00000466222.6:n.1019G>A
ENST00000561817.5:c.101G>A	ENSP00000456575.1:p.Ser34Asn
ENST00000562199.1:n.104G>A
ENST00000564503.5:c.193G>A
ENST00000565274.5:c.308G>A	ENSP00000457759.1:p.Ser103Asn
ENST00000565559.5:c.278G>A	ENSP00000457878.1:p.Ser93Asn
ENST00000569136.5:c.101G>A	ENSP00000455254.1:p.Ser34Asn
ENST00000569827.5:c.428G>A	ENSP00000454379.1:p.Ser143Asn
NM_000070.2:c.2096G>A	NP_000061.1:p.Ser699Asn
NM_024344.1:c.2078G>A	NP_077320.1:p.Ser693Asn
NM_173087.1:c.1820G>A	NP_775110.1:p.Ser607Asn
NM_173088.1:c.560G>A	NP_775111.1:p.Ser187Asn
NM_173089.1:c.101G>A	NP_775112.1:p.Ser34Asn
NM_173090.1:c.101G>A	NP_775113.1:p.Ser34Asn
NM_000070.3:c.2096G>A MANE Select	NP_000061.1:p.Ser699Asn
NM_024344.2:c.2078G>A	NP_077320.1:p.Ser693Asn
NM_173087.2:c.1820G>A	NP_775110.1:p.Ser607Asn
NM_173088.2:c.560G>A	NP_775111.1:p.Ser187Asn
NM_173089.2:c.101G>A	NP_775112.1:p.Ser34Asn
NM_173090.2:c.101G>A	NP_775113.1:p.Ser34Asn