Canonical Allele Identifier: CA63888094
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1265335
ClinVar RCV Id: RCV001678108
dbSNP Id: rs36043647

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201277115T>C , CM000664.2:g.201277115T>C GRCh38
NC_000002.11:g.202141838T>C , CM000664.1:g.202141838T>C GRCh37
NC_000002.10:g.201850083T>C NCBI36
NG_007497.1:g.48658T>C , LRG_34:g.48658T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000413726.6:c.802+147T>C ENSP00000397528.2:n.802+147T>C
ENST00000440732.6:c.802+147T>C ENSP00000396869.2:n.802+147T>C
ENST00000444430.3:c.550+4339T>C ENSP00000394434.3:n.550+4339T>C
ENST00000447616.6:c.*29+147T>C ENSP00000388306.2:n.*29+147T>C
ENST00000450491.6:c.448+147T>C ENSP00000391709.2:n.448+147T>C
ENST00000696067.1:c.802+147T>C ENSP00000512369.1:n.802+147T>C
ENST00000696068.1:c.*29+147T>C ENSP00000512370.1:n.*29+147T>C
ENST00000696069.1:c.757+147T>C ENSP00000512371.1:n.757+147T>C
ENST00000696085.1:c.934+147T>C ENSP00000512381.1:n.934+147T>C
ENST00000696087.1:c.757+147T>C ENSP00000512382.1:n.757+147T>C
ENST00000673742.1:c.802+147T>C MANE Select ENSP00000501268.1:n.802+147T>C
ENST00000264274.13:c.550+4339T>C ENSP00000264274.9:n.550+4339T>C
ENST00000264275.9:c.853+147T>C ENSP00000264275.5:n.853+147T>C
ENST00000323492.11:c.757+147T>C ENSP00000325722.7:n.757+147T>C
ENST00000339403.6:n.1023+11T>C
ENST00000358485.8:c.979+147T>C ENSP00000351273.4:n.979+147T>C
ENST00000392258.7:c.*29+147T>C ENSP00000376087.3:n.*29+147T>C
ENST00000392263.6:c.757+147T>C ENSP00000376091.2:n.757+147T>C
ENST00000392266.7:c.758+146T>C ENSP00000376094.4:n.758+146T>C
ENST00000424461.5:c.281+147T>C ENSP00000390346.1:n.281+147T>C
ENST00000432109.6:c.802+147T>C ENSP00000412523.2:n.802+147T>C
ENST00000444430.2:c.139+4339T>C ENSP00000394434.2:n.139+4339T>C
NM_001080124.1:c.757+147T>C NP_001073593.1:n.757+147T>C
NM_001080125.1:c.979+147T>C NP_001073594.1:n.979+147T>C
NM_001228.4:c.853+147T>C , LRG_34t1:c.853+147T>C NP_001219.2:n.853+147T>C
NM_033355.3:c.802+147T>C , LRG_34t2:c.802+147T>C NP_203519.1:n.802+147T>C
NM_033356.3:c.757+147T>C NP_203520.1:n.757+147T>C
NM_033358.3:c.*29+147T>C NP_203522.1:n.*29+147T>C
NR_111983.1:n.1316+11T>C
XM_005246885.1:c.934+147T>C XP_005246942.1:n.934+147T>C
XM_005246886.1:c.802+147T>C XP_005246943.1:n.802+147T>C
XM_005246887.1:c.802+147T>C XP_005246944.1:n.802+147T>C
XM_005246888.1:c.802+147T>C XP_005246945.1:n.802+147T>C
XM_005246889.1:c.802+147T>C XP_005246946.1:n.802+147T>C
XM_005246890.2:c.802+147T>C XP_005246947.1:n.802+147T>C
XM_005246891.3:c.802+147T>C XP_005246948.1:n.802+147T>C
XM_005246892.1:c.757+147T>C XP_005246949.1:n.757+147T>C
XM_005246893.2:c.*29+147T>C XP_005246950.1:n.*29+147T>C
XM_005246894.2:c.205+147T>C XP_005246951.1:n.205+147T>C
XM_005246895.2:c.*29+147T>C XP_005246952.1:n.*29+147T>C
XM_006712789.1:c.802+147T>C XP_006712852.1:n.802+147T>C
XM_006712790.2:c.802+147T>C XP_006712853.1:n.802+147T>C
XM_006712791.1:c.727+4339T>C XP_006712854.1:n.727+4339T>C
XM_006712793.2:c.*29+147T>C XP_006712856.1:n.*29+147T>C
XM_011511968.1:c.979+147T>C XP_011510270.1:n.979+147T>C
XM_011511969.1:c.367+147T>C XP_011510271.1:n.367+147T>C
XM_011511970.1:c.*29+147T>C XP_011510272.1:n.*29+147T>C
XR_923035.1:n.1071+11T>C
XM_005246885.2:c.934+147T>C XP_005246942.1:n.934+147T>C
XM_005246886.2:c.802+147T>C XP_005246943.1:n.802+147T>C
XM_005246887.2:c.802+147T>C XP_005246944.1:n.802+147T>C
XM_005246888.2:c.802+147T>C XP_005246945.1:n.802+147T>C
XM_005246889.2:c.802+147T>C XP_005246946.1:n.802+147T>C
XM_005246890.4:c.802+147T>C XP_005246947.1:n.802+147T>C
XM_005246891.5:c.802+147T>C XP_005246948.1:n.802+147T>C
XM_005246892.2:c.757+147T>C XP_005246949.1:n.757+147T>C
XM_005246893.3:c.*29+147T>C XP_005246950.1:n.*29+147T>C
XM_005246894.4:c.205+147T>C XP_005246951.1:n.205+147T>C
XM_005246895.3:c.*29+147T>C XP_005246952.1:n.*29+147T>C
XM_006712789.2:c.802+147T>C XP_006712852.1:n.802+147T>C
XM_006712790.4:c.802+147T>C XP_006712853.1:n.802+147T>C
XM_006712793.3:c.*29+147T>C XP_006712856.1:n.*29+147T>C
XM_011511969.2:c.367+147T>C XP_011510271.1:n.367+147T>C
XR_001738971.1:n.1149+11T>C
NM_001080124.2:c.757+147T>C NP_001073593.1:n.757+147T>C
NM_001080125.2:c.979+147T>C NP_001073594.1:n.979+147T>C
NM_001372051.1:c.802+147T>C MANE Select NP_001358980.1:n.802+147T>C
NM_033356.4:c.757+147T>C NP_203520.1:n.757+147T>C
NM_033358.4:c.*29+147T>C NP_203522.1:n.*29+147T>C
NR_111983.2:n.1312+11T>C
NM_001400642.1:c.934+147T>C NP_001387571.1:n.934+147T>C
NM_001400645.1:c.835+147T>C NP_001387574.1:n.835+147T>C
NM_001400648.1:c.802+147T>C NP_001387577.1:n.802+147T>C
NM_001400651.1:c.802+147T>C NP_001387580.1:n.802+147T>C
NM_001400653.1:c.802+147T>C NP_001387582.1:n.802+147T>C
NM_001400654.1:c.802+147T>C NP_001387583.1:n.802+147T>C
NM_001400655.1:c.802+147T>C NP_001387584.1:n.802+147T>C
NM_001400656.1:c.802+147T>C NP_001387585.1:n.802+147T>C
NM_001400657.1:c.802+147T>C NP_001387586.1:n.802+147T>C
NM_001400658.1:c.757+147T>C NP_001387587.1:n.757+147T>C
NM_001400659.1:c.757+147T>C NP_001387588.1:n.757+147T>C
NM_001400660.1:c.757+147T>C NP_001387589.1:n.757+147T>C
NM_001400661.1:c.757+147T>C NP_001387590.1:n.757+147T>C
NM_001400662.1:c.757+147T>C NP_001387591.1:n.757+147T>C
NM_001400663.1:c.757+147T>C NP_001387592.1:n.757+147T>C
NM_001400664.1:c.733+147T>C NP_001387593.1:n.733+147T>C
NM_001400665.1:c.727+4339T>C NP_001387594.1:n.727+4339T>C
NM_001400666.1:c.595+4173T>C NP_001387595.1:n.595+4173T>C
NM_001400667.1:c.550+4339T>C NP_001387596.1:n.550+4339T>C
NM_001400668.1:c.550+4339T>C NP_001387597.1:n.550+4339T>C
NM_001400669.1:c.493+147T>C NP_001387598.1:n.493+147T>C
NM_001400670.1:c.802+147T>C NP_001387599.1:n.802+147T>C
NM_001400671.1:c.205+147T>C NP_001387600.1:n.205+147T>C
NM_001400672.1:c.205+147T>C NP_001387601.1:n.205+147T>C
NM_001400673.1:c.205+147T>C NP_001387602.1:n.205+147T>C
NM_001400674.1:c.187+147T>C NP_001387603.1:n.187+147T>C
NM_001400675.1:c.160+147T>C NP_001387604.1:n.160+147T>C
NM_001400676.1:c.160+147T>C NP_001387605.1:n.160+147T>C
NM_001400677.1:c.160+147T>C NP_001387606.1:n.160+147T>C
NM_001400678.1:c.160+147T>C NP_001387607.1:n.160+147T>C
NM_001400679.1:c.*176T>C NP_001387608.1:n.*176T>C
NM_001400680.1:c.187+147T>C NP_001387609.1:n.187+147T>C
NM_001400750.1:c.205+147T>C NP_001387679.1:n.205+147T>C
NM_001400751.1:c.160+147T>C NP_001387680.1:n.160+147T>C
NR_174564.1:n.891+11T>C
NR_174565.1:n.1021+11T>C
NR_174581.1:n.1047+11T>C
NR_174583.1:n.1153+11T>C
NR_174584.1:n.1066+147T>C
NR_174585.1:n.1084+11T>C
NR_174586.1:n.1058+11T>C
NR_174588.1:n.1221+11T>C
NR_174589.1:n.1016+11T>C
NR_174590.1:n.1108+11T>C
NR_174591.1:n.1039+11T>C
NR_174592.1:n.1384+11T>C
NR_174593.1:n.1182+11T>C
NR_174594.1:n.1225+11T>C
NR_174595.1:n.1140+11T>C
NR_174596.1:n.977+11T>C
NR_174598.1:n.1335+11T>C
NR_174599.1:n.719+2162T>C
NR_174600.1:n.1247+11T>C
NR_174601.1:n.1172+11T>C
NR_174602.1:n.1042+11T>C