Canonical Allele Identifier: CA350294312
Gene: CASP8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201276919G>T , CM000664.2:g.201276919G>T GRCh38
NC_000002.11:g.202141642G>T , CM000664.1:g.202141642G>T GRCh37
NC_000002.10:g.201849887G>T NCBI36
NG_007497.1:g.48462G>T , LRG_34:g.48462G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000413726.6:c.753G>T ENSP00000397528.2:p.Val251=
ENST00000440732.6:c.753G>T ENSP00000396869.2:p.Val251=
ENST00000444430.3:c.550+4143G>T ENSP00000394434.3:n.550+4143G>T
ENST00000447616.6:c.643G>T ENSP00000388306.2:p.Ala215Ser
ENST00000450491.6:c.399G>T ENSP00000391709.2:p.Val133=
ENST00000696067.1:c.753G>T ENSP00000512369.1:p.Val251=
ENST00000696068.1:c.643G>T ENSP00000512370.1:p.Ala215Ser
ENST00000696069.1:c.708G>T ENSP00000512371.1:p.Val236=
ENST00000696085.1:c.885G>T ENSP00000512381.1:p.Val295=
ENST00000696087.1:c.708G>T ENSP00000512382.1:p.Val236=
ENST00000673742.1:c.753G>T MANE Select ENSP00000501268.1:p.Val251=
ENST00000264274.13:c.550+4143G>T ENSP00000264274.9:n.550+4143G>T
ENST00000264275.9:c.804G>T ENSP00000264275.5:p.Val268=
ENST00000323492.11:c.708G>T ENSP00000325722.7:p.Val236=
ENST00000339403.6:n.838G>T
ENST00000358485.8:c.930G>T ENSP00000351273.4:p.Val310=
ENST00000392258.7:c.688G>T ENSP00000376087.3:p.Ala230Ser
ENST00000392263.6:c.708G>T ENSP00000376091.2:p.Val236=
ENST00000392266.7:c.708G>T ENSP00000376094.4:p.Val236=
ENST00000424461.5:c.232G>T ENSP00000390346.1:p.Ala78Ser
ENST00000432109.6:c.753G>T ENSP00000412523.2:p.Val251=
ENST00000444430.2:c.139+4143G>T ENSP00000394434.2:n.139+4143G>T
ENST00000450491.5:c.399G>T ENSP00000391709.1:p.Val133=
NM_001080124.1:c.708G>T NP_001073593.1:p.Val236=
NM_001080125.1:c.930G>T NP_001073594.1:p.Val310=
NM_001228.4:c.804G>T , LRG_34t1:c.804G>T NP_001219.2:p.Val268=
NM_033355.3:c.753G>T , LRG_34t2:c.753G>T NP_203519.1:p.Val251=
NM_033356.3:c.708G>T NP_203520.1:p.Val236=
NM_033358.3:c.688G>T NP_203522.1:p.Ala230Ser
NR_111983.1:n.1131G>T
XM_005246885.1:c.885G>T XP_005246942.1:p.Val295=
XM_005246886.1:c.753G>T XP_005246943.1:p.Val251=
XM_005246887.1:c.753G>T XP_005246944.1:p.Val251=
XM_005246888.1:c.753G>T XP_005246945.1:p.Val251=
XM_005246889.1:c.753G>T XP_005246946.1:p.Val251=
XM_005246890.2:c.753G>T XP_005246947.1:p.Val251=
XM_005246891.3:c.753G>T XP_005246948.1:p.Val251=
XM_005246892.1:c.708G>T XP_005246949.1:p.Val236=
XM_005246893.2:c.865G>T XP_005246950.1:p.Ala289Ser
XM_005246894.2:c.156G>T XP_005246951.1:p.Val52=
XM_005246895.2:c.820G>T XP_005246952.1:p.Ala274Ser
XM_006712789.1:c.753G>T XP_006712852.1:p.Val251=
XM_006712790.2:c.753G>T XP_006712853.1:p.Val251=
XM_006712791.1:c.727+4143G>T XP_006712854.1:n.727+4143G>T
XM_006712793.2:c.688G>T XP_006712856.1:p.Ala230Ser
XM_011511968.1:c.930G>T XP_011510270.1:p.Val310=
XM_011511969.1:c.318G>T XP_011510271.1:p.Val106=
XM_011511970.1:c.865G>T XP_011510272.1:p.Ala289Ser
XR_923035.1:n.886G>T
XM_005246885.2:c.885G>T XP_005246942.1:p.Val295=
XM_005246886.2:c.753G>T XP_005246943.1:p.Val251=
XM_005246887.2:c.753G>T XP_005246944.1:p.Val251=
XM_005246888.2:c.753G>T XP_005246945.1:p.Val251=
XM_005246889.2:c.753G>T XP_005246946.1:p.Val251=
XM_005246890.4:c.753G>T XP_005246947.1:p.Val251=
XM_005246891.5:c.753G>T XP_005246948.1:p.Val251=
XM_005246892.2:c.708G>T XP_005246949.1:p.Val236=
XM_005246893.3:c.865G>T XP_005246950.1:p.Ala289Ser
XM_005246894.4:c.156G>T XP_005246951.1:p.Val52=
XM_005246895.3:c.820G>T XP_005246952.1:p.Ala274Ser
XM_006712789.2:c.753G>T XP_006712852.1:p.Val251=
XM_006712790.4:c.753G>T XP_006712853.1:p.Val251=
XM_006712793.3:c.688G>T XP_006712856.1:p.Ala230Ser
XM_011511969.2:c.318G>T XP_011510271.1:p.Val106=
XR_001738971.1:n.964G>T
NM_001080124.2:c.708G>T NP_001073593.1:p.Val236=
NM_001080125.2:c.930G>T NP_001073594.1:p.Val310=
NM_001372051.1:c.753G>T MANE Select NP_001358980.1:p.Val251=
NM_033356.4:c.708G>T NP_203520.1:p.Val236=
NM_033358.4:c.688G>T NP_203522.1:p.Ala230Ser
NR_111983.2:n.1127G>T
NM_001400642.1:c.885G>T NP_001387571.1:p.Val295=
NM_001400645.1:c.786G>T NP_001387574.1:p.Val262=
NM_001400648.1:c.753G>T NP_001387577.1:p.Val251=
NM_001400651.1:c.753G>T NP_001387580.1:p.Val251=
NM_001400653.1:c.753G>T NP_001387582.1:p.Val251=
NM_001400654.1:c.753G>T NP_001387583.1:p.Val251=
NM_001400655.1:c.753G>T NP_001387584.1:p.Val251=
NM_001400656.1:c.753G>T NP_001387585.1:p.Val251=
NM_001400657.1:c.753G>T NP_001387586.1:p.Val251=
NM_001400658.1:c.708G>T NP_001387587.1:p.Val236=
NM_001400659.1:c.708G>T NP_001387588.1:p.Val236=
NM_001400660.1:c.708G>T NP_001387589.1:p.Val236=
NM_001400661.1:c.708G>T NP_001387590.1:p.Val236=
NM_001400662.1:c.708G>T NP_001387591.1:p.Val236=
NM_001400663.1:c.708G>T NP_001387592.1:p.Val236=
NM_001400664.1:c.684G>T NP_001387593.1:p.Val228=
NM_001400665.1:c.727+4143G>T NP_001387594.1:n.727+4143G>T
NM_001400666.1:c.595+3977G>T NP_001387595.1:n.595+3977G>T
NM_001400667.1:c.550+4143G>T NP_001387596.1:n.550+4143G>T
NM_001400668.1:c.550+4143G>T NP_001387597.1:n.550+4143G>T
NM_001400669.1:c.444G>T NP_001387598.1:p.Val148=
NM_001400670.1:c.753G>T NP_001387599.1:p.Val251=
NM_001400671.1:c.156G>T NP_001387600.1:p.Val52=
NM_001400672.1:c.156G>T NP_001387601.1:p.Val52=
NM_001400673.1:c.156G>T NP_001387602.1:p.Val52=
NM_001400674.1:c.138G>T NP_001387603.1:p.Val46=
NM_001400675.1:c.111G>T NP_001387604.1:p.Val37=
NM_001400676.1:c.111G>T NP_001387605.1:p.Val37=
NM_001400677.1:c.111G>T NP_001387606.1:p.Val37=
NM_001400678.1:c.111G>T NP_001387607.1:p.Val37=
NM_001400679.1:c.688G>T NP_001387608.1:p.Ala230Ser
NM_001400680.1:c.138G>T NP_001387609.1:p.Val46=
NM_001400750.1:c.156G>T NP_001387679.1:p.Val52=
NM_001400751.1:c.111G>T NP_001387680.1:p.Val37=
NR_174564.1:n.706G>T
NR_174565.1:n.836G>T
NR_174581.1:n.862G>T
NR_174583.1:n.968G>T
NR_174584.1:n.1017G>T
NR_174585.1:n.899G>T
NR_174586.1:n.873G>T
NR_174588.1:n.1036G>T
NR_174589.1:n.831G>T
NR_174590.1:n.923G>T
NR_174591.1:n.854G>T
NR_174592.1:n.1199G>T
NR_174593.1:n.997G>T
NR_174594.1:n.1040G>T
NR_174595.1:n.955G>T
NR_174596.1:n.792G>T
NR_174598.1:n.1150G>T
NR_174599.1:n.719+1966G>T
NR_174600.1:n.1062G>T
NR_174601.1:n.987G>T
NR_174602.1:n.857G>T