Canonical Allele Identifier: CA2172718640
Gene: CAPN3 HGNC NCBI

Linked Data

dbSNP Id: rs2053862220

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42401479_42401480insG , CM000677.2:g.42401479_42401480insG GRCh38
NC_000015.9:g.42693677_42693678insG , CM000677.1:g.42693677_42693678insG GRCh37
NC_000015.8:g.40480969_40480970insG NCBI36
NG_008660.1:g.58377_58378insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.1211-162_1211-161insG ENSP00000183936.4:n.1211-162_1211-161insG
ENST00000357568.8:c.1355-162_1355-161insG ENSP00000350181.3:n.1355-162_1355-161insG
ENST00000397163.8:c.1355-162_1355-161insG MANE Select ENSP00000380349.3:n.1355-162_1355-161insG
ENST00000466369.5:n.1864-162_1864-161insG
ENST00000483208.5:n.1586-162_1586-161insG
ENST00000495723.1:n.1586-162_1586-161insG
ENST00000549793.5:n.1586-162_1586-161insG
ENST00000638141.2:n.1226-162_1226-161insG
ENST00000673705.1:c.309+1827_309+1828insG ENSP00000501021.1:n.309+1827_309+1828insG
ENST00000318023.11:c.1211-162_1211-161insG ENSP00000326281.8:n.1211-162_1211-161insG
ENST00000349748.7:c.1211-162_1211-161insG ENSP00000183936.4:n.1211-162_1211-161insG
ENST00000357568.7:c.1355-162_1355-161insG ENSP00000350181.3:n.1355-162_1355-161insG
ENST00000397163.7:c.1355-162_1355-161insG ENSP00000380349.3:n.1355-162_1355-161insG
NM_000070.2:c.1355-162_1355-161insG NP_000061.1:n.1355-162_1355-161insG
NM_024344.1:c.1355-162_1355-161insG NP_077320.1:n.1355-162_1355-161insG
NM_173087.1:c.1211-162_1211-161insG NP_775110.1:n.1211-162_1211-161insG
NM_000070.3:c.1355-162_1355-161insG MANE Select NP_000061.1:n.1355-162_1355-161insG
NM_024344.2:c.1355-162_1355-161insG NP_077320.1:n.1355-162_1355-161insG
NM_173087.2:c.1211-162_1211-161insG NP_775110.1:n.1211-162_1211-161insG