Canonical Allele Identifier: CA1732859377
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915686A= , CM000669.2:g.107915686A= GRCh38
NC_000007.13:g.107556131A= , CM000669.1:g.107556131A= GRCh37
NC_000007.12:g.107343367A= NCBI36
NG_008045.1:g.29546A=

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.865A= MANE Select ENSP00000205402.3:p.Ile289=
ENST00000205402.9:c.865A= ENSP00000205402.3:p.Ile289=
ENST00000415325.5:c.*539A= ENSP00000402593.1:n.*539A=
ENST00000417551.5:c.865A= ENSP00000390667.1:p.Ile289=
ENST00000437604.6:c.721A= ENSP00000387542.2:p.Ile241=
ENST00000440410.5:c.796A= ENSP00000417016.1:p.Ile266=
NM_000108.4:c.865A= NP_000099.2:p.Ile289=
NM_001289750.1:c.568A= NP_001276679.1:p.Ile190=
NM_001289751.1:c.796A= NP_001276680.1:p.Ile266=
NM_001289752.1:c.721A= NP_001276681.1:p.Ile241=
NM_000108.5:c.865A= MANE Select NP_000099.2:p.Ile289=