LDH info

Canonical Allele Identifier: CA262723195

Identifiers and link-outs to other resources

dbSNP Id: rs12894182

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65471171C>A , CM000676.2:g.65471171C>A GRCh38
NC_000014.8:g.65937889C>A , CM000676.1:g.65937889C>A GRCh37
NC_000014.7:g.65007642C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_004480.4:c.-287+15453C>A (FUT8) VV NP_004471.4:p.=
NM_178155.2:c.-228+15453C>A (FUT8) VV NP_835368.1:p.=
NM_178156.2:c.-228+59178C>A (FUT8) VV NP_835369.1:p.=
NR_030355.1:n.70C>A (MIR625)
NR_038167.1:n.1500+15453C>A (FUT8)
NR_038170.1:n.583+15453C>A (FUT8)
XM_011536613.1:c.-228+57957C>A (FUT8) XP_011534915.1:p.=
XM_017021136.1:c.-228+15453C>A (FUT8) XP_016876625.1:p.=
XM_017021137.1:c.-228+15453C>A (FUT8) XP_016876626.1:p.=
XM_017021138.1:c.-228+59178C>A (FUT8) XP_016876627.1:p.=
XM_017021139.1:c.-228+57957C>A (FUT8) XP_016876628.1:p.=
NM_001371533.1:c.-228+15453C>A (FUT8) VV NP_001358462.1:p.=
NM_001371534.1:c.-228+15453C>A (FUT8) VV NP_001358463.1:p.=
NM_001371536.1:c.-228+15453C>A (FUT8) VV NP_001358465.1:p.=
NM_178155.3:c.-228+15453C>A (FUT8) VV NP_835368.1:p.=
ENST00000342677.10:c.-228+15453C>A ENSP00000345865.6:p.=
ENST00000358307.6:c.-287+15453C>A ENSP00000351057.2:p.=
ENST00000360689.9:c.-228+15453C>A ENSP00000353910.5:p.=
ENST00000394586.6:c.-228+59178C>A ENSP00000378087.2:p.=
ENST00000553924.5:c.-374+15453C>A ENSP00000451577.1:p.=
ENST00000554610.1:c.-228+57957C>A ENSP00000452309.1:p.=
ENST00000555559.5:c.-305-8536C>A ENSP00000451689.1:p.=
ENST00000556518.5:c.-228+15453C>A ENSP00000452597.1:p.=
ENST00000557164.5:c.-287+15453C>A ENSP00000452433.1:p.=
ENST00000557338.5:c.-305-8536C>A ENSP00000452105.1:p.=