Canonical Allele Identifier: CA269853961
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42360027T>G , CM000677.2:g.42360027T>G GRCh38
NC_000015.9:g.42652225T>G , CM000677.1:g.42652225T>G GRCh37
NC_000015.8:g.40439517T>G NCBI36
NG_008660.1:g.16925T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.222T>G ENSP00000183936.4:p.Leu74=
ENST00000357568.8:c.222T>G ENSP00000350181.3:p.Leu74=
ENST00000397163.8:c.222T>G MANE Select ENSP00000380349.3:p.Leu74=
ENST00000466369.5:n.540+5574T>G
ENST00000483208.5:n.540+5574T>G
ENST00000495723.1:n.540+5574T>G
ENST00000549793.5:n.540+5574T>G
ENST00000318023.11:c.222T>G ENSP00000326281.8:p.Leu74=
ENST00000349748.7:c.222T>G ENSP00000183936.4:p.Leu74=
ENST00000357568.7:c.222T>G ENSP00000350181.3:p.Leu74=
ENST00000397163.7:c.222T>G ENSP00000380349.3:p.Leu74=
NM_000070.2:c.222T>G NP_000061.1:p.Leu74=
NM_024344.1:c.222T>G NP_077320.1:p.Leu74=
NM_173087.1:c.222T>G NP_775110.1:p.Leu74=
NM_000070.3:c.222T>G MANE Select NP_000061.1:p.Leu74=
NM_024344.2:c.222T>G NP_077320.1:p.Leu74=
NM_173087.2:c.222T>G NP_775110.1:p.Leu74=