Canonical Allele Identifier: CA1320996726
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287710T= , CM000664.2:g.201287710T= GRCh38
NC_000002.11:g.202152433T= , CM000664.1:g.202152433T= GRCh37
NC_000002.10:g.201860678T= NCBI36
NG_007497.1:g.59253T= , LRG_34:g.59253T=

Transcript Alleles

HGVS Amino-acid change
ENST00000444430.3:c.2304T= ENSP00000394434.3:n.2304T=
ENST00000696069.1:c.1259+2393T= ENSP00000512371.1:n.1259+2393T=
ENST00000264274.13:c.*1116T= ENSP00000264274.9:n.*1116T=
ENST00000358485.8:c.*1116T= ENSP00000351273.4:n.*1116T=
NM_001080124.1:c.*1116T= NP_001073593.1:n.*1116T=
NM_001080125.1:c.*1116T= NP_001073594.1:n.*1116T=
NM_001228.4:c.*1116T= , LRG_34t1:c.*1116T= NP_001219.2:n.*1116T=
NM_033355.3:c.*1116T= , LRG_34t2:c.*1116T= NP_203519.1:n.*1116T=
NM_033356.3:c.*1116T= NP_203520.1:n.*1116T=
NR_111983.1:n.3070T=
XM_005246885.1:c.*1116T= XP_005246942.1:n.*1116T=
XM_005246886.1:c.*1116T= XP_005246943.1:n.*1116T=
XM_005246887.1:c.*1116T= XP_005246944.1:n.*1116T=
XM_005246888.1:c.*1116T= XP_005246945.1:n.*1116T=
XM_005246889.1:c.*1116T= XP_005246946.1:n.*1116T=
XM_005246890.2:c.*1116T= XP_005246947.1:n.*1116T=
XM_005246891.3:c.*1116T= XP_005246948.1:n.*1116T=
XM_005246892.1:c.*1116T= XP_005246949.1:n.*1116T=
XM_005246894.2:c.*1116T= XP_005246951.1:n.*1116T=
XM_006712789.1:c.*1116T= XP_006712852.1:n.*1116T=
XM_006712790.2:c.*1116T= XP_006712853.1:n.*1116T=
XM_006712791.1:c.*1116T= XP_006712854.1:n.*1116T=
XM_011511969.1:c.*1116T= XP_011510271.1:n.*1116T=