Canonical Allele Identifier: CA1320996730

Gene: CASP8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287711T= , CM000664.2:g.201287711T=	GRCh38
NC_000002.11:g.202152434T= , CM000664.1:g.202152434T=	GRCh37
NC_000002.10:g.201860679T=	NCBI36
NG_007497.1:g.59254T= , LRG_34:g.59254T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000444430.3:c.2305T=	ENSP00000394434.3:n.2305T=
ENST00000696069.1:c.1259+2394T=	ENSP00000512371.1:n.1259+2394T=
ENST00000264274.13:c.*1117T=	ENSP00000264274.9:n.*1117T=
ENST00000358485.8:c.*1117T=	ENSP00000351273.4:n.*1117T=
NM_001080124.1:c.*1117T=	NP_001073593.1:n.*1117T=
NM_001080125.1:c.*1117T=	NP_001073594.1:n.*1117T=
NM_001228.4:c.*1117T= , LRG_34t1:c.*1117T=	NP_001219.2:n.*1117T=
NM_033355.3:c.*1117T= , LRG_34t2:c.*1117T=	NP_203519.1:n.*1117T=
NM_033356.3:c.*1117T=	NP_203520.1:n.*1117T=
NR_111983.1:n.3071T=
XM_005246885.1:c.*1117T=	XP_005246942.1:n.*1117T=
XM_005246886.1:c.*1117T=	XP_005246943.1:n.*1117T=
XM_005246887.1:c.*1117T=	XP_005246944.1:n.*1117T=
XM_005246888.1:c.*1117T=	XP_005246945.1:n.*1117T=
XM_005246889.1:c.*1117T=	XP_005246946.1:n.*1117T=
XM_005246890.2:c.*1117T=	XP_005246947.1:n.*1117T=
XM_005246891.3:c.*1117T=	XP_005246948.1:n.*1117T=
XM_005246892.1:c.*1117T=	XP_005246949.1:n.*1117T=
XM_005246894.2:c.*1117T=	XP_005246951.1:n.*1117T=
XM_006712789.1:c.*1117T=	XP_006712852.1:n.*1117T=
XM_006712790.2:c.*1117T=	XP_006712853.1:n.*1117T=
XM_006712791.1:c.*1117T=	XP_006712854.1:n.*1117T=
XM_011511969.1:c.*1117T=	XP_011510271.1:n.*1117T=