Canonical Allele Identifier: CA1320967271
Gene: CASP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201209209T= , CM000664.2:g.201209209T= GRCh38
NC_000002.11:g.202073932T= , CM000664.1:g.202073932T= GRCh37
NC_000002.10:g.201782177T= NCBI36
NG_007265.1:g.31078T= , LRG_33:g.31078T=

Transcript Alleles

HGVS Amino-acid change
ENST00000313728.12:c.861T= ENSP00000314599.7:p.Cys287=
ENST00000346817.10:c.933T= ENSP00000237865.7:p.Cys311=
ENST00000438843.6:c.*519T= ENSP00000401914.1:n.*519T=
ENST00000492363.6:c.*148T= ENSP00000512459.1:n.*148T=
ENST00000696199.1:c.721+5443T= ENSP00000512481.1:n.721+5443T=
ENST00000286186.11:c.1062T= MANE Select ENSP00000286186.6:p.Cys354=
ENST00000272879.9:c.1062T= ENSP00000272879.5:p.Cys354=
ENST00000286186.10:c.1062T= ENSP00000286186.6:p.Cys354=
ENST00000313728.11:c.861T= ENSP00000314599.7:p.Cys287=
ENST00000346817.9:c.933T= ENSP00000237865.7:p.Cys311=
ENST00000360132.7:c.*148T= ENSP00000353250.3:n.*148T=
ENST00000448480.1:c.933T= ENSP00000396835.1:p.Cys311=
ENST00000492363.5:n.970T=
NM_001206524.1:c.861T= NP_001193453.1:p.Cys287=
NM_001206542.1:c.933T= NP_001193471.1:p.Cys311=
NM_001230.4:c.933T= NP_001221.2:p.Cys311=
NM_032974.4:c.1062T= NP_116756.2:p.Cys354=
NM_032976.3:c.*148T= NP_116758.1:n.*148T=
NM_032977.3:c.1062T= , LRG_33t1:c.1062T= NP_116759.2:p.Cys354=
XM_005246907.2:c.1059T= XP_005246964.1:p.Cys353=
XM_006712796.2:c.312T= XP_006712859.1:p.Cys104=
XM_006712796.3:c.312T= XP_006712859.1:p.Cys104=
NM_001206524.2:c.861T= NP_001193453.1:p.Cys287=
NM_001206542.2:c.933T= NP_001193471.1:p.Cys311=
NM_001230.5:c.933T= NP_001221.2:p.Cys311=
NM_032974.5:c.1062T= NP_116756.2:p.Cys354=
NM_032977.4:c.1062T= MANE Select NP_116759.2:p.Cys354=
NM_032976.4:c.*148T= NP_116758.1:n.*148T=