LDH info

Canonical Allele Identifier: CA15217195
Gene: CASP8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6704688

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201241309C>T , CM000664.2:g.201241309C>T GRCh38
NC_000002.11:g.202106032C>T , CM000664.1:g.202106032C>T GRCh37
NC_000002.10:g.201814277C>T NCBI36
NG_007497.1:g.12852C>T , LRG_34:g.12852C>T

Transcript Alleles

HGVS Amino-acid change
NM_001080124.1:c.-27+7197C>T VV NP_001073593.1:p.=
NM_001228.4:c.-27+7197C>T , LRG_34t1:c.-27+7197C>T NP_001219.2:p.=
NM_033355.3:c.-1+7197C>T , LRG_34t2:c.-1+7197C>T NP_203519.1:p.=
NM_033358.3:c.-27+7197C>T VV NP_203522.1:p.=
XM_005246887.1:c.-27+7197C>T XP_005246944.1:p.=
XM_005246888.1:c.-1+7197C>T XP_005246945.1:p.=
XM_005246894.2:c.-559+7197C>T XP_005246951.1:p.=
XM_006712789.1:c.-27+7197C>T XP_006712852.1:p.=
XM_006712793.2:c.-27+7197C>T XP_006712856.1:p.=
XM_005246887.2:c.-27+7197C>T XP_005246944.1:p.=
XM_005246888.2:c.-1+7197C>T XP_005246945.1:p.=
XM_005246894.4:c.-559+7197C>T XP_005246951.1:p.=
XM_006712789.2:c.-27+7197C>T XP_006712852.1:p.=
XM_006712793.3:c.-27+7197C>T XP_006712856.1:p.=
XR_001738971.1:n.250+7197C>T
NM_001080124.2:c.-27+7197C>T VV NP_001073593.1:p.=
NM_033358.4:c.-27+7197C>T VV NP_203522.1:p.=
ENST00000264274.13:c.-27+7197C>T ENSP00000264274.9:p.=
ENST00000264275.9:c.-27+7197C>T ENSP00000264275.5:p.=
ENST00000392258.7:c.-27+7197C>T ENSP00000376087.3:p.=
ENST00000392263.6:c.-27+7197C>T ENSP00000376091.2:p.=
ENST00000432109.6:c.-1+7197C>T ENSP00000412523.2:p.=
ENST00000440732.5:c.-1+7197C>T ENSP00000396869.1:p.=
ENST00000450491.5:c.-5+7197C>T ENSP00000391709.1:p.=
ENST00000471383.5:n.250+7197C>T
ENST00000490682.5:n.1295C>T