Canonical Allele Identifier: CA381252306

Gene: CAPN1

Linked Data

• MyVariant Identifiers: chr11:g.64974250G>A (hg19) ; chr11:g.65206779G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65206779G>A , CM000673.2:g.65206779G>A	GRCh38
NC_000011.9:g.64974250G>A , CM000673.1:g.64974250G>A	GRCh37
NC_000011.8:g.64730826G>A	NCBI36
NG_052817.1:g.30565G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279247.11:c.1566-1G>A MANE Select	ENSP00000279247.7:n.1566-1G>A
ENST00000279247.10:c.1566-1G>A	ENSP00000279247.6:n.1566-1G>A
ENST00000524773.5:c.1566-1G>A	ENSP00000434176.1:n.1566-1G>A
ENST00000525013.1:n.419-1G>A
ENST00000527323.5:c.1566-1G>A	ENSP00000431984.1:n.1566-1G>A
ENST00000533129.5:c.1566-1G>A	ENSP00000431686.1:n.1566-1G>A
ENST00000533820.5:c.1566-1G>A	ENSP00000435272.1:n.1566-1G>A
NM_001198868.1:c.1566-1G>A	NP_001185797.1:n.1566-1G>A
NM_001198869.1:c.1566-1G>A	NP_001185798.1:n.1566-1G>A
NM_005186.3:c.1566-1G>A	NP_005177.2:n.1566-1G>A
NR_040008.1:n.1678-1G>A
XM_006718698.1:c.1566-1G>A	XP_006718761.1:n.1566-1G>A
XM_011545292.1:c.1566-1G>A	XP_011543594.1:n.1566-1G>A
XM_006718698.2:c.1566-1G>A	XP_006718761.1:n.1566-1G>A
NM_001198868.2:c.1566-1G>A	NP_001185797.1:n.1566-1G>A
NM_005186.4:c.1566-1G>A MANE Select	NP_005177.2:n.1566-1G>A
NR_040008.2:n.1583-1G>A
NM_001198869.2:c.1566-1G>A	NP_001185798.1:n.1566-1G>A