Canonical Allele Identifier: CA63887912
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs570153139

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201276948A>G , CM000664.2:g.201276948A>G GRCh38
NC_000002.11:g.202141671A>G , CM000664.1:g.202141671A>G GRCh37
NC_000002.10:g.201849916A>G NCBI36
NG_007497.1:g.48491A>G , LRG_34:g.48491A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000413726.6:c.782A>G ENSP00000397528.2:p.Asn261Ser
ENST00000440732.6:c.782A>G ENSP00000396869.2:p.Asn261Ser
ENST00000444430.3:c.550+4172A>G ENSP00000394434.3:n.550+4172A>G
ENST00000447616.6:c.*9A>G ENSP00000388306.2:n.*9A>G
ENST00000450491.6:c.428A>G ENSP00000391709.2:p.Asn143Ser
ENST00000696067.1:c.782A>G ENSP00000512369.1:p.Asn261Ser
ENST00000696068.1:c.*9A>G ENSP00000512370.1:n.*9A>G
ENST00000696069.1:c.737A>G ENSP00000512371.1:p.Asn246Ser
ENST00000696085.1:c.914A>G ENSP00000512381.1:p.Asn305Ser
ENST00000696087.1:c.737A>G ENSP00000512382.1:p.Asn246Ser
ENST00000673742.1:c.782A>G MANE Select ENSP00000501268.1:p.Asn261Ser
ENST00000264274.13:c.550+4172A>G ENSP00000264274.9:n.550+4172A>G
ENST00000264275.9:c.833A>G ENSP00000264275.5:p.Asn278Ser
ENST00000323492.11:c.737A>G ENSP00000325722.7:p.Asn246Ser
ENST00000339403.6:n.867A>G
ENST00000358485.8:c.959A>G ENSP00000351273.4:p.Asn320Ser
ENST00000392258.7:c.*9A>G ENSP00000376087.3:n.*9A>G
ENST00000392263.6:c.737A>G ENSP00000376091.2:p.Asn246Ser
ENST00000392266.7:c.737A>G ENSP00000376094.4:p.Asn246Ser
ENST00000424461.5:c.261A>G ENSP00000390346.1:n.261A>G
ENST00000432109.6:c.782A>G ENSP00000412523.2:p.Asn261Ser
ENST00000444430.2:c.139+4172A>G ENSP00000394434.2:n.139+4172A>G
ENST00000450491.5:c.428A>G ENSP00000391709.1:p.Asn143Ser
NM_001080124.1:c.737A>G NP_001073593.1:p.Asn246Ser
NM_001080125.1:c.959A>G NP_001073594.1:p.Asn320Ser
NM_001228.4:c.833A>G , LRG_34t1:c.833A>G NP_001219.2:p.Asn278Ser
NM_033355.3:c.782A>G , LRG_34t2:c.782A>G NP_203519.1:p.Asn261Ser
NM_033356.3:c.737A>G NP_203520.1:p.Asn246Ser
NM_033358.3:c.*9A>G NP_203522.1:n.*9A>G
NR_111983.1:n.1160A>G
XM_005246885.1:c.914A>G XP_005246942.1:p.Asn305Ser
XM_005246886.1:c.782A>G XP_005246943.1:p.Asn261Ser
XM_005246887.1:c.782A>G XP_005246944.1:p.Asn261Ser
XM_005246888.1:c.782A>G XP_005246945.1:p.Asn261Ser
XM_005246889.1:c.782A>G XP_005246946.1:p.Asn261Ser
XM_005246890.2:c.782A>G XP_005246947.1:p.Asn261Ser
XM_005246891.3:c.782A>G XP_005246948.1:p.Asn261Ser
XM_005246892.1:c.737A>G XP_005246949.1:p.Asn246Ser
XM_005246893.2:c.*9A>G XP_005246950.1:n.*9A>G
XM_005246894.2:c.185A>G XP_005246951.1:p.Asn62Ser
XM_005246895.2:c.*9A>G XP_005246952.1:n.*9A>G
XM_006712789.1:c.782A>G XP_006712852.1:p.Asn261Ser
XM_006712790.2:c.782A>G XP_006712853.1:p.Asn261Ser
XM_006712791.1:c.727+4172A>G XP_006712854.1:n.727+4172A>G
XM_006712793.2:c.*9A>G XP_006712856.1:n.*9A>G
XM_011511968.1:c.959A>G XP_011510270.1:p.Asn320Ser
XM_011511969.1:c.347A>G XP_011510271.1:p.Asn116Ser
XM_011511970.1:c.*9A>G XP_011510272.1:n.*9A>G
XR_923035.1:n.915A>G
XM_005246885.2:c.914A>G XP_005246942.1:p.Asn305Ser
XM_005246886.2:c.782A>G XP_005246943.1:p.Asn261Ser
XM_005246887.2:c.782A>G XP_005246944.1:p.Asn261Ser
XM_005246888.2:c.782A>G XP_005246945.1:p.Asn261Ser
XM_005246889.2:c.782A>G XP_005246946.1:p.Asn261Ser
XM_005246890.4:c.782A>G XP_005246947.1:p.Asn261Ser
XM_005246891.5:c.782A>G XP_005246948.1:p.Asn261Ser
XM_005246892.2:c.737A>G XP_005246949.1:p.Asn246Ser
XM_005246893.3:c.*9A>G XP_005246950.1:n.*9A>G
XM_005246894.4:c.185A>G XP_005246951.1:p.Asn62Ser
XM_005246895.3:c.*9A>G XP_005246952.1:n.*9A>G
XM_006712789.2:c.782A>G XP_006712852.1:p.Asn261Ser
XM_006712790.4:c.782A>G XP_006712853.1:p.Asn261Ser
XM_006712793.3:c.*9A>G XP_006712856.1:n.*9A>G
XM_011511969.2:c.347A>G XP_011510271.1:p.Asn116Ser
XR_001738971.1:n.993A>G
NM_001080124.2:c.737A>G NP_001073593.1:p.Asn246Ser
NM_001080125.2:c.959A>G NP_001073594.1:p.Asn320Ser
NM_001372051.1:c.782A>G MANE Select NP_001358980.1:p.Asn261Ser
NM_033356.4:c.737A>G NP_203520.1:p.Asn246Ser
NM_033358.4:c.*9A>G NP_203522.1:n.*9A>G
NR_111983.2:n.1156A>G
NM_001400642.1:c.914A>G NP_001387571.1:p.Asn305Ser
NM_001400645.1:c.815A>G NP_001387574.1:p.Asn272Ser
NM_001400648.1:c.782A>G NP_001387577.1:p.Asn261Ser
NM_001400651.1:c.782A>G NP_001387580.1:p.Asn261Ser
NM_001400653.1:c.782A>G NP_001387582.1:p.Asn261Ser
NM_001400654.1:c.782A>G NP_001387583.1:p.Asn261Ser
NM_001400655.1:c.782A>G NP_001387584.1:p.Asn261Ser
NM_001400656.1:c.782A>G NP_001387585.1:p.Asn261Ser
NM_001400657.1:c.782A>G NP_001387586.1:p.Asn261Ser
NM_001400658.1:c.737A>G NP_001387587.1:p.Asn246Ser
NM_001400659.1:c.737A>G NP_001387588.1:p.Asn246Ser
NM_001400660.1:c.737A>G NP_001387589.1:p.Asn246Ser
NM_001400661.1:c.737A>G NP_001387590.1:p.Asn246Ser
NM_001400662.1:c.737A>G NP_001387591.1:p.Asn246Ser
NM_001400663.1:c.737A>G NP_001387592.1:p.Asn246Ser
NM_001400664.1:c.713A>G NP_001387593.1:p.Asn238Ser
NM_001400665.1:c.727+4172A>G NP_001387594.1:n.727+4172A>G
NM_001400666.1:c.595+4006A>G NP_001387595.1:n.595+4006A>G
NM_001400667.1:c.550+4172A>G NP_001387596.1:n.550+4172A>G
NM_001400668.1:c.550+4172A>G NP_001387597.1:n.550+4172A>G
NM_001400669.1:c.473A>G NP_001387598.1:p.Asn158Ser
NM_001400670.1:c.782A>G NP_001387599.1:p.Asn261Ser
NM_001400671.1:c.185A>G NP_001387600.1:p.Asn62Ser
NM_001400672.1:c.185A>G NP_001387601.1:p.Asn62Ser
NM_001400673.1:c.185A>G NP_001387602.1:p.Asn62Ser
NM_001400674.1:c.167A>G NP_001387603.1:p.Asn56Ser
NM_001400675.1:c.140A>G NP_001387604.1:p.Asn47Ser
NM_001400676.1:c.140A>G NP_001387605.1:p.Asn47Ser
NM_001400677.1:c.140A>G NP_001387606.1:p.Asn47Ser
NM_001400678.1:c.140A>G NP_001387607.1:p.Asn47Ser
NM_001400679.1:c.*9A>G NP_001387608.1:n.*9A>G
NM_001400680.1:c.167A>G NP_001387609.1:p.Asn56Ser
NM_001400750.1:c.185A>G NP_001387679.1:p.Asn62Ser
NM_001400751.1:c.140A>G NP_001387680.1:p.Asn47Ser
NR_174564.1:n.735A>G
NR_174565.1:n.865A>G
NR_174581.1:n.891A>G
NR_174583.1:n.997A>G
NR_174584.1:n.1046A>G
NR_174585.1:n.928A>G
NR_174586.1:n.902A>G
NR_174588.1:n.1065A>G
NR_174589.1:n.860A>G
NR_174590.1:n.952A>G
NR_174591.1:n.883A>G
NR_174592.1:n.1228A>G
NR_174593.1:n.1026A>G
NR_174594.1:n.1069A>G
NR_174595.1:n.984A>G
NR_174596.1:n.821A>G
NR_174598.1:n.1179A>G
NR_174599.1:n.719+1995A>G
NR_174600.1:n.1091A>G
NR_174601.1:n.1016A>G
NR_174602.1:n.886A>G