Canonical Allele Identifier: CA391997457

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42386165A>G , CM000677.2:g.42386165A>G	GRCh38
NC_000015.9:g.42678363A>G , CM000677.1:g.42678363A>G	GRCh37
NC_000015.8:g.40465655A>G	NCBI36
NG_008660.1:g.43063A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000070.3:c.380-2A>G MANE Select	NP_000061.1:n.380-2A>G
ENST00000397163.8:c.380-2A>G MANE Select	ENSP00000380349.3:n.380-2A>G
NM_000070.2:c.380-2A>G	NP_000061.1:n.380-2A>G
NM_024344.1:c.380-2A>G	NP_077320.1:n.380-2A>G
NM_024344.2:c.380-2A>G	NP_077320.1:n.380-2A>G
NM_173087.1:c.380-2A>G	NP_775110.1:n.380-2A>G
NM_173087.2:c.380-2A>G	NP_775110.1:n.380-2A>G
ENST00000318023.11:c.380-2A>G	ENSP00000326281.8:n.380-2A>G
ENST00000349748.7:c.380-2A>G	ENSP00000183936.4:n.380-2A>G
ENST00000349748.8:c.380-2A>G	ENSP00000183936.4:n.380-2A>G
ENST00000357568.7:c.380-2A>G	ENSP00000350181.3:n.380-2A>G
ENST00000357568.8:c.380-2A>G	ENSP00000350181.3:n.380-2A>G
ENST00000397163.7:c.380-2A>G	ENSP00000380349.3:n.380-2A>G
ENST00000466369.5:n.889-2A>G
ENST00000483208.5:n.611-2A>G
ENST00000495723.1:n.611-2A>G
ENST00000549793.5:n.611-2A>G
ENST00000638141.2:n.395-2A>G
ENST00000673705.1:c.70+1613A>G	ENSP00000501021.1:n.70+1613A>G