Canonical Allele Identifier: CA350286808
Gene: CASP10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201208159A>T , CM000664.2:g.201208159A>T GRCh38
NC_000002.11:g.202072882A>T , CM000664.1:g.202072882A>T GRCh37
NC_000002.10:g.201781127A>T NCBI36
NG_007265.1:g.30028A>T , LRG_33:g.30028A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.722-911A>T ENSP00000314599.7:n.722-911A>T
ENST00000346817.10:c.769A>T ENSP00000237865.7:p.Arg257Ter
ENST00000438843.6:c.*355A>T ENSP00000401914.1:n.*355A>T
ENST00000492363.6:c.806A>T ENSP00000512459.1:p.Gln269Leu
ENST00000696199.1:c.721+4393A>T ENSP00000512481.1:n.721+4393A>T
ENST00000286186.11:c.898A>T MANE Select ENSP00000286186.6:p.Arg300Ter
ENST00000272879.9:c.898A>T ENSP00000272879.5:p.Arg300Ter
ENST00000286186.10:c.898A>T ENSP00000286186.6:p.Arg300Ter
ENST00000313728.11:c.722-911A>T ENSP00000314599.7:n.722-911A>T
ENST00000346817.9:c.769A>T ENSP00000237865.7:p.Arg257Ter
ENST00000360132.7:c.806A>T ENSP00000353250.3:p.Gln269Leu
ENST00000438843.5:c.*355A>T ENSP00000401914.1:n.*355A>T
ENST00000448480.1:c.769A>T ENSP00000396835.1:p.Arg257Ter
ENST00000492363.5:n.806A>T
NM_001206524.1:c.722-911A>T NP_001193453.1:n.722-911A>T
NM_001206542.1:c.769A>T NP_001193471.1:p.Arg257Ter
NM_001230.4:c.769A>T NP_001221.2:p.Arg257Ter
NM_032974.4:c.898A>T NP_116756.2:p.Arg300Ter
NM_032976.3:c.806A>T NP_116758.1:p.Gln269Leu
NM_032977.3:c.898A>T , LRG_33t1:c.898A>T NP_116759.2:p.Arg300Ter
XM_005246907.2:c.895A>T XP_005246964.1:p.Arg299Ter
XM_006712796.2:c.148A>T XP_006712859.1:p.Arg50Ter
XM_011511990.1:c.803A>T XP_011510292.1:p.Gln268Leu
XR_923043.1:n.1102A>T
XR_923044.1:n.1010A>T
XM_006712796.3:c.148A>T XP_006712859.1:p.Arg50Ter
XM_011511990.2:c.803A>T XP_011510292.1:p.Gln268Leu
XR_923043.2:n.1102A>T
XR_923044.2:n.1010A>T
NM_001206524.2:c.722-911A>T NP_001193453.1:n.722-911A>T
NM_001206542.2:c.769A>T NP_001193471.1:p.Arg257Ter
NM_001230.5:c.769A>T NP_001221.2:p.Arg257Ter
NM_032974.5:c.898A>T NP_116756.2:p.Arg300Ter
NM_032977.4:c.898A>T MANE Select NP_116759.2:p.Arg300Ter
NM_032976.4:c.806A>T NP_116758.1:p.Gln269Leu