Canonical Allele Identifier: CA2662631188

Gene: CASP10

Linked Data

• gnomAD v4: 2-201209474-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209475del , CM000664.2:g.201209475del	GRCh38
NC_000002.11:g.202074198del , CM000664.1:g.202074198del	GRCh37
NC_000002.10:g.201782443del	NCBI36
NG_007265.1:g.31344del , LRG_33:g.31344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1127del	ENSP00000314599.7:p.Val376AlafsTer24
ENST00000346817.10:c.1199del	ENSP00000237865.7:p.Val400AlafsTer24
ENST00000438843.6:c.*785del	ENSP00000401914.1:n.*785del
ENST00000492363.6:c.*414del	ENSP00000512459.1:n.*414del
ENST00000696199.1:c.721+5709del	ENSP00000512481.1:n.721+5709del
ENST00000286186.11:c.1328del MANE Select	ENSP00000286186.6:p.Val443AlafsTer24
ENST00000272879.9:c.1328del	ENSP00000272879.5:p.Val443AlafsTer24
ENST00000286186.10:c.1328del	ENSP00000286186.6:p.Val443AlafsTer24
ENST00000313728.11:c.1127del	ENSP00000314599.7:p.Val376AlafsTer24
ENST00000346817.9:c.1199del	ENSP00000237865.7:p.Val400AlafsTer24
ENST00000360132.7:c.*414del	ENSP00000353250.3:n.*414del
ENST00000448480.1:c.1199del	ENSP00000396835.1:p.Val400AlafsTer24
ENST00000492363.5:n.1236del
NM_001206524.1:c.1127del	NP_001193453.1:p.Val376AlafsTer24
NM_001206542.1:c.1199del	NP_001193471.1:p.Val400AlafsTer24
NM_001230.4:c.1199del	NP_001221.2:p.Val400AlafsTer24
NM_032974.4:c.1328del	NP_116756.2:p.Val443AlafsTer24
NM_032976.3:c.*414del	NP_116758.1:n.*414del
NM_032977.3:c.1328del , LRG_33t1:c.1328del	NP_116759.2:p.Val443AlafsTer24
XM_005246907.2:c.1325del	XP_005246964.1:p.Val442AlafsTer24
XM_006712796.2:c.578del	XP_006712859.1:p.Val193AlafsTer24
XM_006712796.3:c.578del	XP_006712859.1:p.Val193AlafsTer24
NM_001206524.2:c.1127del	NP_001193453.1:p.Val376AlafsTer24
NM_001206542.2:c.1199del	NP_001193471.1:p.Val400AlafsTer24
NM_001230.5:c.1199del	NP_001221.2:p.Val400AlafsTer24
NM_032974.5:c.1328del	NP_116756.2:p.Val443AlafsTer24
NM_032977.4:c.1328del MANE Select	NP_116759.2:p.Val443AlafsTer24
NM_032976.4:c.*414del	NP_116758.1:n.*414del