Canonical Allele Identifier: CA10604967
Gene: CAPN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 284946
dbSNP Id: rs779701414

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42388928G>C , CM000677.2:g.42388928G>C GRCh38
NC_000015.9:g.42681126G>C , CM000677.1:g.42681126G>C GRCh37
NC_000015.8:g.40468418G>C NCBI36
NG_008660.1:g.45826G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.633G>C ENSP00000183936.4:p.Lys211Asn
ENST00000357568.8:c.633G>C ENSP00000350181.3:p.Lys211Asn
ENST00000397163.8:c.633G>C MANE Select ENSP00000380349.3:p.Lys211Asn
ENST00000466369.5:n.1142G>C
ENST00000483208.5:n.864G>C
ENST00000495723.1:n.864G>C
ENST00000549793.5:n.864G>C
ENST00000638141.2:n.648G>C
ENST00000673705.1:c.70+4376G>C ENSP00000501021.1:n.70+4376G>C
ENST00000318023.11:c.633G>C ENSP00000326281.8:p.Lys211Asn
ENST00000349748.7:c.633G>C ENSP00000183936.4:p.Lys211Asn
ENST00000357568.7:c.633G>C ENSP00000350181.3:p.Lys211Asn
ENST00000397163.7:c.633G>C ENSP00000380349.3:p.Lys211Asn
NM_000070.2:c.633G>C NP_000061.1:p.Lys211Asn
NM_024344.1:c.633G>C NP_077320.1:p.Lys211Asn
NM_173087.1:c.633G>C NP_775110.1:p.Lys211Asn
NM_000070.3:c.633G>C MANE Select NP_000061.1:p.Lys211Asn
NM_024344.2:c.633G>C NP_077320.1:p.Lys211Asn
NM_173087.2:c.633G>C NP_775110.1:p.Lys211Asn