Canonical Allele Identifier: CA919540242

Gene: CAPN3

Linked Data

• dbSNP Id: rs1595826427

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42392451_42392465del , CM000677.2:g.42392451_42392465del	GRCh38
NC_000015.9:g.42684649_42684663del , CM000677.1:g.42684649_42684663del	GRCh37
NC_000015.8:g.40471941_40471955del	NCBI36
NG_008660.1:g.49349_49363del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.802-188_802-174del	ENSP00000183936.4:n.802-188_802-174del
ENST00000357568.8:c.946-188_946-174del	ENSP00000350181.3:n.946-188_946-174del
ENST00000397163.8:c.946-188_946-174del MANE Select	ENSP00000380349.3:n.946-188_946-174del
ENST00000466369.5:n.1455-188_1455-174del
ENST00000483208.5:n.1177-188_1177-174del
ENST00000495723.1:n.1177-188_1177-174del
ENST00000549793.5:n.1177-188_1177-174del
ENST00000638141.2:n.817-188_817-174del
ENST00000673705.1:c.71-4349_71-4335del	ENSP00000501021.1:n.71-4349_71-4335del
ENST00000318023.11:c.802-188_802-174del	ENSP00000326281.8:n.802-188_802-174del
ENST00000349748.7:c.802-188_802-174del	ENSP00000183936.4:n.802-188_802-174del
ENST00000357568.7:c.946-188_946-174del	ENSP00000350181.3:n.946-188_946-174del
ENST00000397163.7:c.946-188_946-174del	ENSP00000380349.3:n.946-188_946-174del
NM_000070.2:c.946-188_946-174del	NP_000061.1:n.946-188_946-174del
NM_024344.1:c.946-188_946-174del	NP_077320.1:n.946-188_946-174del
NM_173087.1:c.802-188_802-174del	NP_775110.1:n.802-188_802-174del
NM_000070.3:c.946-188_946-174del MANE Select	NP_000061.1:n.946-188_946-174del
NM_024344.2:c.946-188_946-174del	NP_077320.1:n.946-188_946-174del
NM_173087.2:c.802-188_802-174del	NP_775110.1:n.802-188_802-174del