Canonical Allele Identifier: CA2662631192

Gene: CASP10

Linked Data

• gnomAD v4: 2-201209556-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209559del , CM000664.2:g.201209559del	GRCh38
NC_000002.11:g.202074282del , CM000664.1:g.202074282del	GRCh37
NC_000002.10:g.201782527del	NCBI36
NG_007265.1:g.31428del , LRG_33:g.31428del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1211del	ENSP00000314599.7:p.Pro404GlnfsTer17
ENST00000346817.10:c.1283del	ENSP00000237865.7:p.Pro428GlnfsTer17
ENST00000438843.6:c.*869del	ENSP00000401914.1:n.*869del
ENST00000492363.6:c.*498del	ENSP00000512459.1:n.*498del
ENST00000696199.1:c.721+5793del	ENSP00000512481.1:n.721+5793del
ENST00000286186.11:c.1412del MANE Select	ENSP00000286186.6:p.Pro471GlnfsTer17
ENST00000272879.9:c.1412del	ENSP00000272879.5:p.Pro471GlnfsTer4
ENST00000286186.10:c.1412del	ENSP00000286186.6:p.Pro471GlnfsTer17
ENST00000313728.11:c.1211del	ENSP00000314599.7:p.Pro404GlnfsTer17
ENST00000346817.9:c.1283del	ENSP00000237865.7:p.Pro428GlnfsTer17
ENST00000360132.7:c.*498del	ENSP00000353250.3:n.*498del
ENST00000448480.1:c.1283del	ENSP00000396835.1:p.Pro428GlnfsTer4
ENST00000492363.5:n.1320del
NM_001206524.1:c.1211del	NP_001193453.1:p.Pro404GlnfsTer17
NM_001206542.1:c.1283del	NP_001193471.1:p.Pro428GlnfsTer4
NM_001230.4:c.1283del	NP_001221.2:p.Pro428GlnfsTer17
NM_032974.4:c.1412del	NP_116756.2:p.Pro471GlnfsTer4
NM_032976.3:c.*498del	NP_116758.1:n.*498del
NM_032977.3:c.1412del , LRG_33t1:c.1412del	NP_116759.2:p.Pro471GlnfsTer17
XM_005246907.2:c.1409del	XP_005246964.1:p.Pro470GlnfsTer17
XM_006712796.2:c.662del	XP_006712859.1:p.Pro221GlnfsTer17
XM_006712796.3:c.662del	XP_006712859.1:p.Pro221GlnfsTer17
NM_001206524.2:c.1211del	NP_001193453.1:p.Pro404GlnfsTer17
NM_001206542.2:c.1283del	NP_001193471.1:p.Pro428GlnfsTer4
NM_001230.5:c.1283del	NP_001221.2:p.Pro428GlnfsTer17
NM_032974.5:c.1412del	NP_116756.2:p.Pro471GlnfsTer4
NM_032977.4:c.1412del MANE Select	NP_116759.2:p.Pro471GlnfsTer17
NM_032976.4:c.*498del	NP_116758.1:n.*498del