Canonical Allele Identifier: CA712902952

Gene: CAPN3

Linked Data

• dbSNP Id: rs963647313
• MyVariant Identifiers: chr15:g.42694194C>G (hg19) ; chr15:g.42401996C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42401996C>G , CM000677.2:g.42401996C>G	GRCh38
NC_000015.9:g.42694194C>G , CM000677.1:g.42694194C>G	GRCh37
NC_000015.8:g.40481486C>G	NCBI36
NG_008660.1:g.58894C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1381-128C>G	ENSP00000183936.4:n.1381-128C>G
ENST00000357568.8:c.1525-128C>G	ENSP00000350181.3:n.1525-128C>G
ENST00000397163.8:c.1525-128C>G MANE Select	ENSP00000380349.3:n.1525-128C>G
ENST00000466369.5:n.2034-128C>G
ENST00000483208.5:n.1756-128C>G
ENST00000495723.1:n.1756-128C>G
ENST00000549793.5:n.1756-128C>G
ENST00000638141.2:n.1396-128C>G
ENST00000673705.1:c.309+2344C>G	ENSP00000501021.1:n.309+2344C>G
ENST00000673813.1:n.23+68C>G
ENST00000318023.11:c.1381-128C>G	ENSP00000326281.8:n.1381-128C>G
ENST00000349748.7:c.1381-128C>G	ENSP00000183936.4:n.1381-128C>G
ENST00000357568.7:c.1525-128C>G	ENSP00000350181.3:n.1525-128C>G
ENST00000397163.7:c.1525-128C>G	ENSP00000380349.3:n.1525-128C>G
NM_000070.2:c.1525-128C>G	NP_000061.1:n.1525-128C>G
NM_024344.1:c.1525-128C>G	NP_077320.1:n.1525-128C>G
NM_173087.1:c.1381-128C>G	NP_775110.1:n.1381-128C>G
NM_000070.3:c.1525-128C>G MANE Select	NP_000061.1:n.1525-128C>G
NM_024344.2:c.1525-128C>G	NP_077320.1:n.1525-128C>G
NM_173087.2:c.1381-128C>G	NP_775110.1:n.1381-128C>G