Canonical Allele Identifier: CA2172719397
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42401968_42401969delinsCA , CM000677.2:g.42401968_42401969delinsCA GRCh38
NC_000015.9:g.42694166_42694167delinsCA , CM000677.1:g.42694166_42694167delinsCA GRCh37
NC_000015.8:g.40481458_40481459delinsCA NCBI36
NG_008660.1:g.58866_58867delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.1381-156_1381-155delinsCA ENSP00000183936.4:n.1381-156_1381-155delinsCA
ENST00000357568.8:c.1525-156_1525-155delinsCA ENSP00000350181.3:n.1525-156_1525-155delinsCA
ENST00000397163.8:c.1525-156_1525-155delinsCA MANE Select ENSP00000380349.3:n.1525-156_1525-155delinsCA
ENST00000466369.5:n.2034-156_2034-155delinsCA
ENST00000483208.5:n.1756-156_1756-155delinsCA
ENST00000495723.1:n.1756-156_1756-155delinsCA
ENST00000549793.5:n.1756-156_1756-155delinsCA
ENST00000638141.2:n.1396-156_1396-155delinsCA
ENST00000673705.1:c.309+2316_309+2317delinsCA ENSP00000501021.1:n.309+2316_309+2317delinsCA
ENST00000673813.1:n.23+40_23+41delinsCA
ENST00000318023.11:c.1381-156_1381-155delinsCA ENSP00000326281.8:n.1381-156_1381-155delinsCA
ENST00000349748.7:c.1381-156_1381-155delinsCA ENSP00000183936.4:n.1381-156_1381-155delinsCA
ENST00000357568.7:c.1525-156_1525-155delinsCA ENSP00000350181.3:n.1525-156_1525-155delinsCA
ENST00000397163.7:c.1525-156_1525-155delinsCA ENSP00000380349.3:n.1525-156_1525-155delinsCA
NM_000070.2:c.1525-156_1525-155delinsCA NP_000061.1:n.1525-156_1525-155delinsCA
NM_024344.1:c.1525-156_1525-155delinsCA NP_077320.1:n.1525-156_1525-155delinsCA
NM_173087.1:c.1381-156_1381-155delinsCA NP_775110.1:n.1381-156_1381-155delinsCA
NM_000070.3:c.1525-156_1525-155delinsCA MANE Select NP_000061.1:n.1525-156_1525-155delinsCA
NM_024344.2:c.1525-156_1525-155delinsCA NP_077320.1:n.1525-156_1525-155delinsCA
NM_173087.2:c.1381-156_1381-155delinsCA NP_775110.1:n.1381-156_1381-155delinsCA