Canonical Allele Identifier: CA1732859373
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915678A= , CM000669.2:g.107915678A= GRCh38
NC_000007.13:g.107556123A= , CM000669.1:g.107556123A= GRCh37
NC_000007.12:g.107343359A= NCBI36
NG_008045.1:g.29538A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.857A= MANE Select ENSP00000205402.3:p.Asp286=
ENST00000205402.9:c.857A= ENSP00000205402.3:p.Asp286=
ENST00000415325.5:c.*531A= ENSP00000402593.1:n.*531A=
ENST00000417551.5:c.857A= ENSP00000390667.1:p.Asp286=
ENST00000437604.6:c.713A= ENSP00000387542.2:p.Asp238=
ENST00000440410.5:c.788A= ENSP00000417016.1:p.Asp263=
NM_000108.4:c.857A= NP_000099.2:p.Asp286=
NM_001289750.1:c.560A= NP_001276679.1:p.Asp187=
NM_001289751.1:c.788A= NP_001276680.1:p.Asp263=
NM_001289752.1:c.713A= NP_001276681.1:p.Asp238=
NM_000108.5:c.857A= MANE Select NP_000099.2:p.Asp286=