LDH info

Canonical Allele Identifier: CA11094797
Gene: CASP8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3817578

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201271872C>T , CM000664.2:g.201271872C>T GRCh38
NC_000002.11:g.202136595C>T , CM000664.1:g.202136595C>T GRCh37
NC_000002.10:g.201844840C>T NCBI36
NG_007497.1:g.43415C>T , LRG_34:g.43415C>T

Transcript Alleles

HGVS Amino-acid change
NM_001080124.1:c.411+251C>T VV NP_001073593.1:p.=
NM_001080125.1:c.588+251C>T VV NP_001073594.1:p.=
NM_001228.4:c.507+251C>T , LRG_34t1:c.507+251C>T NP_001219.2:p.=
NM_033355.3:c.411+251C>T , LRG_34t2:c.411+251C>T NP_203519.1:p.=
NM_033356.3:c.411+251C>T VV NP_203520.1:p.=
NM_033358.3:c.411+251C>T VV NP_203522.1:p.=
NR_111983.1:n.789+251C>T
XM_005246885.1:c.588+251C>T XP_005246942.1:p.=
XM_005246886.1:c.411+251C>T XP_005246943.1:p.=
XM_005246887.1:c.411+251C>T XP_005246944.1:p.=
XM_005246888.1:c.411+251C>T XP_005246945.1:p.=
XM_005246889.1:c.411+251C>T XP_005246946.1:p.=
XM_005246890.2:c.411+251C>T XP_005246947.1:p.=
XM_005246891.3:c.411+251C>T XP_005246948.1:p.=
XM_005246892.1:c.411+251C>T XP_005246949.1:p.=
XM_005246893.2:c.588+251C>T XP_005246950.1:p.=
XM_005246894.2:c.-122+251C>T XP_005246951.1:p.=
XM_005246895.2:c.588+251C>T XP_005246952.1:p.=
XM_006712789.1:c.411+251C>T XP_006712852.1:p.=
XM_006712790.2:c.411+251C>T XP_006712853.1:p.=
XM_006712791.1:c.588+251C>T XP_006712854.1:p.=
XM_006712793.2:c.411+251C>T XP_006712856.1:p.=
XM_011511968.1:c.588+251C>T XP_011510270.1:p.=
XM_011511969.1:c.-24-766C>T XP_011510271.1:p.=
XM_011511970.1:c.588+251C>T XP_011510272.1:p.=
XR_923035.1:n.609+251C>T
XM_005246885.2:c.588+251C>T XP_005246942.1:p.=
XM_005246886.2:c.411+251C>T XP_005246943.1:p.=
XM_005246887.2:c.411+251C>T XP_005246944.1:p.=
XM_005246888.2:c.411+251C>T XP_005246945.1:p.=
XM_005246889.2:c.411+251C>T XP_005246946.1:p.=
XM_005246890.4:c.411+251C>T XP_005246947.1:p.=
XM_005246891.5:c.411+251C>T XP_005246948.1:p.=
XM_005246892.2:c.411+251C>T XP_005246949.1:p.=
XM_005246893.3:c.588+251C>T XP_005246950.1:p.=
XM_005246894.4:c.-122+251C>T XP_005246951.1:p.=
XM_005246895.3:c.588+251C>T XP_005246952.1:p.=
XM_006712789.2:c.411+251C>T XP_006712852.1:p.=
XM_006712790.4:c.411+251C>T XP_006712853.1:p.=
XM_006712793.3:c.411+251C>T XP_006712856.1:p.=
XM_011511969.2:c.-24-766C>T XP_011510271.1:p.=
XR_001738971.1:n.687+251C>T
ENST00000264274.13:c.411+251C>T ENSP00000264274.9:p.=
ENST00000264275.9:c.507+251C>T ENSP00000264275.5:p.=
ENST00000323492.11:c.411+251C>T ENSP00000325722.7:p.=
ENST00000339403.6:n.496+251C>T
ENST00000358485.8:c.588+251C>T ENSP00000351273.4:p.=
ENST00000392258.7:c.411+251C>T ENSP00000376087.3:p.=
ENST00000392263.6:c.411+251C>T ENSP00000376091.2:p.=
ENST00000392266.7:c.411+251C>T ENSP00000376094.4:p.=
ENST00000413726.5:c.411+251C>T ENSP00000397528.1:p.=
ENST00000432109.6:c.411+251C>T ENSP00000412523.2:p.=
ENST00000437283.5:c.*385+251C>T ENSP00000407378.1:p.=
ENST00000447616.5:c.411+251C>T ENSP00000388306.1:p.=
ENST00000450491.5:c.102+251C>T ENSP00000391709.1:p.=
ENST00000471383.5:n.687+251C>T
ENST00000490412.5:n.142+251C>T