Canonical Allele Identifier: CA2695220006
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42403000dup , CM000677.2:g.42403000dup GRCh38
NC_000015.9:g.42695198dup , CM000677.1:g.42695198dup GRCh37
NC_000015.8:g.40482490dup NCBI36
NG_008660.1:g.59898dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.1599dup ENSP00000183936.4:p.Glu534Ter
ENST00000357568.8:c.1743dup ENSP00000350181.3:p.Glu582Ter
ENST00000397163.8:c.1743dup MANE Select ENSP00000380349.3:p.Glu582Ter
ENST00000466369.5:n.2252dup
ENST00000483208.5:n.2632dup
ENST00000495723.1:n.2632dup
ENST00000549793.5:n.1974dup
ENST00000638141.2:n.1614dup
ENST00000673646.1:c.207dup ENSP00000501007.1:p.Glu70Ter
ENST00000673705.1:c.309+3348dup ENSP00000501021.1:n.309+3348dup
ENST00000673813.1:n.580+85dup
ENST00000318023.11:c.1599dup ENSP00000326281.8:p.Glu534Ter
ENST00000349748.7:c.1599dup ENSP00000183936.4:p.Glu534Ter
ENST00000357568.7:c.1743dup ENSP00000350181.3:p.Glu582Ter
ENST00000397163.7:c.1743dup ENSP00000380349.3:p.Glu582Ter
ENST00000397200.8:c.207dup ENSP00000380384.4:p.Glu70Ter
ENST00000567071.5:c.202dup
ENST00000569827.5:c.207dup ENSP00000454379.1:p.Glu70Ter
NM_000070.2:c.1743dup NP_000061.1:p.Glu582Ter
NM_024344.1:c.1743dup NP_077320.1:p.Glu582Ter
NM_173087.1:c.1599dup NP_775110.1:p.Glu534Ter
NM_173088.1:c.207dup NP_775111.1:p.Glu70Ter
NM_000070.3:c.1743dup MANE Select NP_000061.1:p.Glu582Ter
NM_024344.2:c.1743dup NP_077320.1:p.Glu582Ter
NM_173087.2:c.1599dup NP_775110.1:p.Glu534Ter
NM_173088.2:c.207dup NP_775111.1:p.Glu70Ter