Canonical Allele Identifier: CA269833695

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42386184G>A , CM000677.2:g.42386184G>A	GRCh38
NC_000015.9:g.42678382G>A , CM000677.1:g.42678382G>A	GRCh37
NC_000015.8:g.40465674G>A	NCBI36
NG_008660.1:g.43082G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000070.3:c.397G>A MANE Select	NP_000061.1:p.Ala133Thr
ENST00000397163.8:c.397G>A MANE Select	ENSP00000380349.3:p.Ala133Thr
NM_000070.2:c.397G>A	NP_000061.1:p.Ala133Thr
NM_024344.1:c.397G>A	NP_077320.1:p.Ala133Thr
NM_024344.2:c.397G>A	NP_077320.1:p.Ala133Thr
NM_173087.1:c.397G>A	NP_775110.1:p.Ala133Thr
NM_173087.2:c.397G>A	NP_775110.1:p.Ala133Thr
ENST00000318023.11:c.397G>A	ENSP00000326281.8:p.Ala133Thr
ENST00000349748.7:c.397G>A	ENSP00000183936.4:p.Ala133Thr
ENST00000349748.8:c.397G>A	ENSP00000183936.4:p.Ala133Thr
ENST00000357568.7:c.397G>A	ENSP00000350181.3:p.Ala133Thr
ENST00000357568.8:c.397G>A	ENSP00000350181.3:p.Ala133Thr
ENST00000397163.7:c.397G>A	ENSP00000380349.3:p.Ala133Thr
ENST00000466369.5:n.906G>A
ENST00000483208.5:n.628G>A
ENST00000495723.1:n.628G>A
ENST00000549793.5:n.628G>A
ENST00000638141.2:n.412G>A
ENST00000673705.1:c.70+1632G>A	ENSP00000501021.1:n.70+1632G>A