Canonical Allele Identifier: CA391999700

Gene: CAPN3

Linked Data

• MyVariant Identifiers: chr15:g.42693856C>A (hg19) ; chr15:g.42401658C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42401658C>A , CM000677.2:g.42401658C>A	GRCh38
NC_000015.9:g.42693856C>A , CM000677.1:g.42693856C>A	GRCh37
NC_000015.8:g.40481148C>A	NCBI36
NG_008660.1:g.58556C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000349748.8:c.1228C>A	ENSP00000183936.4:p.Pro410Thr
ENST00000357568.8:c.1372C>A	ENSP00000350181.3:p.Pro458Thr
ENST00000397163.8:c.1372C>A MANE Select	ENSP00000380349.3:p.Pro458Thr
ENST00000466369.5:n.1881C>A
ENST00000483208.5:n.1603C>A
ENST00000495723.1:n.1603C>A
ENST00000549793.5:n.1603C>A
ENST00000638141.2:n.1243C>A
ENST00000673705.1:c.309+2006C>A	ENSP00000501021.1:n.309+2006C>A
ENST00000318023.11:c.1228C>A	ENSP00000326281.8:p.Pro410Thr
ENST00000349748.7:c.1228C>A	ENSP00000183936.4:p.Pro410Thr
ENST00000357568.7:c.1372C>A	ENSP00000350181.3:p.Pro458Thr
ENST00000397163.7:c.1372C>A	ENSP00000380349.3:p.Pro458Thr
NM_000070.2:c.1372C>A	NP_000061.1:p.Pro458Thr
NM_024344.1:c.1372C>A	NP_077320.1:p.Pro458Thr
NM_173087.1:c.1228C>A	NP_775110.1:p.Pro410Thr
NM_000070.3:c.1372C>A MANE Select	NP_000061.1:p.Pro458Thr
NM_024344.2:c.1372C>A	NP_077320.1:p.Pro458Thr
NM_173087.2:c.1228C>A	NP_775110.1:p.Pro410Thr