Canonical Allele Identifier: CA489885188

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 2906657
• ClinVar RCV Id: RCV003632725
• MyVariant Identifiers: chr15:g.42695192C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402994C>T , CM000677.2:g.42402994C>T	GRCh38
NC_000015.9:g.42695192C>T , CM000677.1:g.42695192C>T	GRCh37
NC_000015.8:g.40482484C>T	NCBI36
NG_008660.1:g.59892C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1593C>T	ENSP00000183936.4:p.Asn531=
ENST00000357568.8:c.1737C>T	ENSP00000350181.3:p.Asn579=
ENST00000397163.8:c.1737C>T MANE Select	ENSP00000380349.3:p.Asn579=
ENST00000466369.5:n.2246C>T
ENST00000483208.5:n.2626C>T
ENST00000495723.1:n.2626C>T
ENST00000549793.5:n.1968C>T
ENST00000638141.2:n.1608C>T
ENST00000673646.1:c.201C>T	ENSP00000501007.1:p.Asn67=
ENST00000673705.1:c.309+3342C>T	ENSP00000501021.1:n.309+3342C>T
ENST00000673813.1:n.580+79C>T
ENST00000318023.11:c.1593C>T	ENSP00000326281.8:p.Asn531=
ENST00000349748.7:c.1593C>T	ENSP00000183936.4:p.Asn531=
ENST00000357568.7:c.1737C>T	ENSP00000350181.3:p.Asn579=
ENST00000397163.7:c.1737C>T	ENSP00000380349.3:p.Asn579=
ENST00000397200.8:c.201C>T	ENSP00000380384.4:p.Asn67=
ENST00000567071.5:c.196C>T
ENST00000569827.5:c.201C>T	ENSP00000454379.1:p.Asn67=
NM_000070.2:c.1737C>T	NP_000061.1:p.Asn579=
NM_024344.1:c.1737C>T	NP_077320.1:p.Asn579=
NM_173087.1:c.1593C>T	NP_775110.1:p.Asn531=
NM_173088.1:c.201C>T	NP_775111.1:p.Asn67=
NM_000070.3:c.1737C>T MANE Select	NP_000061.1:p.Asn579=
NM_024344.2:c.1737C>T	NP_077320.1:p.Asn579=
NM_173087.2:c.1593C>T	NP_775110.1:p.Asn531=
NM_173088.2:c.201C>T	NP_775111.1:p.Asn67=