Canonical Allele Identifier: CA1041239022
Gene: CASP10 HGNC NCBI

Linked Data

dbSNP Id: rs1945328553

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201209551del , CM000664.2:g.201209551del GRCh38
NC_000002.11:g.202074274del , CM000664.1:g.202074274del GRCh37
NC_000002.10:g.201782519del NCBI36
NG_007265.1:g.31420del , LRG_33:g.31420del

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.1203del ENSP00000314599.7:p.Lys401AsnfsTer20
ENST00000346817.10:c.1275del ENSP00000237865.7:p.Lys425AsnfsTer20
ENST00000438843.6:c.*861del ENSP00000401914.1:n.*861del
ENST00000492363.6:c.*490del ENSP00000512459.1:n.*490del
ENST00000696199.1:c.721+5785del ENSP00000512481.1:n.721+5785del
ENST00000286186.11:c.1404del MANE Select ENSP00000286186.6:p.Lys468AsnfsTer20
ENST00000272879.9:c.1404del ENSP00000272879.5:p.Lys468AsnfsTer7
ENST00000286186.10:c.1404del ENSP00000286186.6:p.Lys468AsnfsTer20
ENST00000313728.11:c.1203del ENSP00000314599.7:p.Lys401AsnfsTer20
ENST00000346817.9:c.1275del ENSP00000237865.7:p.Lys425AsnfsTer20
ENST00000360132.7:c.*490del ENSP00000353250.3:n.*490del
ENST00000448480.1:c.1275del ENSP00000396835.1:p.Lys425AsnfsTer7
ENST00000492363.5:n.1312del
NM_001206524.1:c.1203del NP_001193453.1:p.Lys401AsnfsTer20
NM_001206542.1:c.1275del NP_001193471.1:p.Lys425AsnfsTer7
NM_001230.4:c.1275del NP_001221.2:p.Lys425AsnfsTer20
NM_032974.4:c.1404del NP_116756.2:p.Lys468AsnfsTer7
NM_032976.3:c.*490del NP_116758.1:n.*490del
NM_032977.3:c.1404del , LRG_33t1:c.1404del NP_116759.2:p.Lys468AsnfsTer20
XM_005246907.2:c.1401del XP_005246964.1:p.Lys467AsnfsTer20
XM_006712796.2:c.654del XP_006712859.1:p.Lys218AsnfsTer20
XM_006712796.3:c.654del XP_006712859.1:p.Lys218AsnfsTer20
NM_001206524.2:c.1203del NP_001193453.1:p.Lys401AsnfsTer20
NM_001206542.2:c.1275del NP_001193471.1:p.Lys425AsnfsTer7
NM_001230.5:c.1275del NP_001221.2:p.Lys425AsnfsTer20
NM_032974.5:c.1404del NP_116756.2:p.Lys468AsnfsTer7
NM_032977.4:c.1404del MANE Select NP_116759.2:p.Lys468AsnfsTer20
NM_032976.4:c.*490del NP_116758.1:n.*490del