Canonical Allele Identifier: CA2753865064

Gene: CASP8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287693A>T , CM000664.2:g.201287693A>T	GRCh38
NC_000002.11:g.202152416A>T , CM000664.1:g.202152416A>T	GRCh37
NC_000002.10:g.201860661A>T	NCBI36
NG_007497.1:g.59236A>T , LRG_34:g.59236A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444430.3:c.2287A>T	ENSP00000394434.3:n.2287A>T
ENST00000696069.1:c.1259+2376A>T	ENSP00000512371.1:n.1259+2376A>T
ENST00000673742.1:c.*1099A>T MANE Select	ENSP00000501268.1:n.*1099A>T
ENST00000264274.13:c.*1099A>T	ENSP00000264274.9:n.*1099A>T
ENST00000323492.11:c.*1099A>T	ENSP00000325722.7:n.*1099A>T
ENST00000358485.8:c.*1099A>T	ENSP00000351273.4:n.*1099A>T
NM_001080124.1:c.*1099A>T	NP_001073593.1:n.*1099A>T
NM_001080125.1:c.*1099A>T	NP_001073594.1:n.*1099A>T
NM_001228.4:c.*1099A>T , LRG_34t1:c.*1099A>T	NP_001219.2:n.*1099A>T
NM_033355.3:c.*1099A>T , LRG_34t2:c.*1099A>T	NP_203519.1:n.*1099A>T
NM_033356.3:c.*1099A>T	NP_203520.1:n.*1099A>T
NR_111983.1:n.3053A>T
XM_005246885.1:c.*1099A>T	XP_005246942.1:n.*1099A>T
XM_005246886.1:c.*1099A>T	XP_005246943.1:n.*1099A>T
XM_005246887.1:c.*1099A>T	XP_005246944.1:n.*1099A>T
XM_005246888.1:c.*1099A>T	XP_005246945.1:n.*1099A>T
XM_005246889.1:c.*1099A>T	XP_005246946.1:n.*1099A>T
XM_005246890.2:c.*1099A>T	XP_005246947.1:n.*1099A>T
XM_005246891.3:c.*1099A>T	XP_005246948.1:n.*1099A>T
XM_005246892.1:c.*1099A>T	XP_005246949.1:n.*1099A>T
XM_005246894.2:c.*1099A>T	XP_005246951.1:n.*1099A>T
XM_006712789.1:c.*1099A>T	XP_006712852.1:n.*1099A>T
XM_006712790.2:c.*1099A>T	XP_006712853.1:n.*1099A>T
XM_006712791.1:c.*1099A>T	XP_006712854.1:n.*1099A>T
XM_011511969.1:c.*1099A>T	XP_011510271.1:n.*1099A>T
NM_001080124.2:c.*1099A>T	NP_001073593.1:n.*1099A>T
NM_001080125.2:c.*1099A>T	NP_001073594.1:n.*1099A>T
NM_001372051.1:c.*1099A>T MANE Select	NP_001358980.1:n.*1099A>T
NM_033356.4:c.*1099A>T	NP_203520.1:n.*1099A>T
NR_111983.2:n.3049A>T
NM_001400642.1:c.*1099A>T	NP_001387571.1:n.*1099A>T
NM_001400645.1:c.*1099A>T	NP_001387574.1:n.*1099A>T
NM_001400648.1:c.*1099A>T	NP_001387577.1:n.*1099A>T
NM_001400651.1:c.*1099A>T	NP_001387580.1:n.*1099A>T
NM_001400653.1:c.*1099A>T	NP_001387582.1:n.*1099A>T
NM_001400654.1:c.*1099A>T	NP_001387583.1:n.*1099A>T
NM_001400655.1:c.*1099A>T	NP_001387584.1:n.*1099A>T
NM_001400656.1:c.*1099A>T	NP_001387585.1:n.*1099A>T
NM_001400657.1:c.*1099A>T	NP_001387586.1:n.*1099A>T
NM_001400658.1:c.*1099A>T	NP_001387587.1:n.*1099A>T
NM_001400659.1:c.*1099A>T	NP_001387588.1:n.*1099A>T
NM_001400660.1:c.*1099A>T	NP_001387589.1:n.*1099A>T
NM_001400661.1:c.*1099A>T	NP_001387590.1:n.*1099A>T
NM_001400662.1:c.*1099A>T	NP_001387591.1:n.*1099A>T
NM_001400663.1:c.*1099A>T	NP_001387592.1:n.*1099A>T
NM_001400664.1:c.*1099A>T	NP_001387593.1:n.*1099A>T
NM_001400665.1:c.*1099A>T	NP_001387594.1:n.*1099A>T
NM_001400666.1:c.*1099A>T	NP_001387595.1:n.*1099A>T
NM_001400667.1:c.*1099A>T	NP_001387596.1:n.*1099A>T
NM_001400668.1:c.*1099A>T	NP_001387597.1:n.*1099A>T
NM_001400669.1:c.*1099A>T	NP_001387598.1:n.*1099A>T
NM_001400670.1:c.*1099A>T	NP_001387599.1:n.*1099A>T
NM_001400671.1:c.*1099A>T	NP_001387600.1:n.*1099A>T
NM_001400672.1:c.*1099A>T	NP_001387601.1:n.*1099A>T
NM_001400673.1:c.*1099A>T	NP_001387602.1:n.*1099A>T
NM_001400674.1:c.*1099A>T	NP_001387603.1:n.*1099A>T
NM_001400675.1:c.*1099A>T	NP_001387604.1:n.*1099A>T
NM_001400676.1:c.*1099A>T	NP_001387605.1:n.*1099A>T
NM_001400677.1:c.*1099A>T	NP_001387606.1:n.*1099A>T
NM_001400678.1:c.*1099A>T	NP_001387607.1:n.*1099A>T
NM_001400680.1:c.*1099A>T	NP_001387609.1:n.*1099A>T
NM_001400750.1:c.*1099A>T	NP_001387679.1:n.*1099A>T
NM_001400751.1:c.*1099A>T	NP_001387680.1:n.*1099A>T
NR_174564.1:n.2628A>T
NR_174565.1:n.2758A>T
NR_174581.1:n.2784A>T
NR_174583.1:n.2890A>T
NR_174584.1:n.2803A>T
NR_174585.1:n.2821A>T
NR_174586.1:n.2795A>T
NR_174588.1:n.2958A>T
NR_174589.1:n.2753A>T
NR_174590.1:n.2845A>T
NR_174591.1:n.2776A>T
NR_174592.1:n.3121A>T
NR_174593.1:n.2919A>T
NR_174594.1:n.2962A>T
NR_174595.1:n.2877A>T
NR_174596.1:n.2714A>T
NR_174598.1:n.3072A>T
NR_174599.1:n.2456A>T
NR_174600.1:n.2984A>T
NR_174601.1:n.2909A>T
NR_174602.1:n.2779A>T