Canonical Allele Identifier: CA350293283

Gene: CASP10

Linked Data

• COSMIC: COSM6156600 ; COSM6156601
• MyVariant Identifiers: chr2:g.202074263C>G (hg19) ; chr2:g.201209540C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209540C>G , CM000664.2:g.201209540C>G	GRCh38
NC_000002.11:g.202074263C>G , CM000664.1:g.202074263C>G	GRCh37
NC_000002.10:g.201782508C>G	NCBI36
NG_007265.1:g.31409C>G , LRG_33:g.31409C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1192C>G	ENSP00000314599.7:p.His398Asp
ENST00000346817.10:c.1264C>G	ENSP00000237865.7:p.His422Asp
ENST00000438843.6:c.*850C>G	ENSP00000401914.1:n.*850C>G
ENST00000492363.6:c.*479C>G	ENSP00000512459.1:n.*479C>G
ENST00000696199.1:c.721+5774C>G	ENSP00000512481.1:n.721+5774C>G
ENST00000286186.11:c.1393C>G MANE Select	ENSP00000286186.6:p.His465Asp
ENST00000272879.9:c.1393C>G	ENSP00000272879.5:p.His465Asp
ENST00000286186.10:c.1393C>G	ENSP00000286186.6:p.His465Asp
ENST00000313728.11:c.1192C>G	ENSP00000314599.7:p.His398Asp
ENST00000346817.9:c.1264C>G	ENSP00000237865.7:p.His422Asp
ENST00000360132.7:c.*479C>G	ENSP00000353250.3:n.*479C>G
ENST00000448480.1:c.1264C>G	ENSP00000396835.1:p.His422Asp
ENST00000492363.5:n.1301C>G
NM_001206524.1:c.1192C>G	NP_001193453.1:p.His398Asp
NM_001206542.1:c.1264C>G	NP_001193471.1:p.His422Asp
NM_001230.4:c.1264C>G	NP_001221.2:p.His422Asp
NM_032974.4:c.1393C>G	NP_116756.2:p.His465Asp
NM_032976.3:c.*479C>G	NP_116758.1:n.*479C>G
NM_032977.3:c.1393C>G , LRG_33t1:c.1393C>G	NP_116759.2:p.His465Asp
XM_005246907.2:c.1390C>G	XP_005246964.1:p.His464Asp
XM_006712796.2:c.643C>G	XP_006712859.1:p.His215Asp
XM_006712796.3:c.643C>G	XP_006712859.1:p.His215Asp
NM_001206524.2:c.1192C>G	NP_001193453.1:p.His398Asp
NM_001206542.2:c.1264C>G	NP_001193471.1:p.His422Asp
NM_001230.5:c.1264C>G	NP_001221.2:p.His422Asp
NM_032974.5:c.1393C>G	NP_116756.2:p.His465Asp
NM_032977.4:c.1393C>G MANE Select	NP_116759.2:p.His465Asp
NM_032976.4:c.*479C>G	NP_116758.1:n.*479C>G