Canonical Allele Identifier: CA391995284
Gene: CAPN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42360098T>A , CM000677.2:g.42360098T>A GRCh38
NC_000015.9:g.42652296T>A , CM000677.1:g.42652296T>A GRCh37
NC_000015.8:g.40439588T>A NCBI36
NG_008660.1:g.16996T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.293T>A ENSP00000183936.4:p.Val98Asp
ENST00000357568.8:c.293T>A ENSP00000350181.3:p.Val98Asp
ENST00000397163.8:c.293T>A MANE Select ENSP00000380349.3:p.Val98Asp
ENST00000466369.5:n.540+5645T>A
ENST00000483208.5:n.540+5645T>A
ENST00000495723.1:n.540+5645T>A
ENST00000549793.5:n.540+5645T>A
ENST00000318023.11:c.293T>A ENSP00000326281.8:p.Val98Asp
ENST00000349748.7:c.293T>A ENSP00000183936.4:p.Val98Asp
ENST00000357568.7:c.293T>A ENSP00000350181.3:p.Val98Asp
ENST00000397163.7:c.293T>A ENSP00000380349.3:p.Val98Asp
NM_000070.2:c.293T>A NP_000061.1:p.Val98Asp
NM_024344.1:c.293T>A NP_077320.1:p.Val98Asp
NM_173087.1:c.293T>A NP_775110.1:p.Val98Asp
NM_000070.3:c.293T>A MANE Select NP_000061.1:p.Val98Asp
NM_024344.2:c.293T>A NP_077320.1:p.Val98Asp
NM_173087.2:c.293T>A NP_775110.1:p.Val98Asp