Canonical Allele Identifier: CA368858600
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917445G>C , CM000669.2:g.107917445G>C GRCh38
NC_000007.13:g.107557890G>C , CM000669.1:g.107557890G>C GRCh37
NC_000007.12:g.107345126G>C NCBI36
NG_008045.1:g.31305G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1219G>C MANE Select ENSP00000205402.3:p.Glu407Gln
ENST00000205402.9:c.1219G>C ENSP00000205402.3:p.Glu407Gln
ENST00000415325.5:c.*893G>C ENSP00000402593.1:n.*893G>C
ENST00000417551.5:c.1219G>C ENSP00000390667.1:p.Glu407Gln
ENST00000437604.6:c.1075G>C ENSP00000387542.2:p.Glu359Gln
ENST00000440410.5:c.1150G>C ENSP00000417016.1:p.Glu384Gln
NM_000108.4:c.1219G>C NP_000099.2:p.Glu407Gln
NM_001289750.1:c.922G>C NP_001276679.1:p.Glu308Gln
NM_001289751.1:c.1150G>C NP_001276680.1:p.Glu384Gln
NM_001289752.1:c.1075G>C NP_001276681.1:p.Glu359Gln
NM_000108.5:c.1219G>C MANE Select NP_000099.2:p.Glu407Gln