Canonical Allele Identifier: CA1732860077
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917441A= , CM000669.2:g.107917441A= GRCh38
NC_000007.13:g.107557886A= , CM000669.1:g.107557886A= GRCh37
NC_000007.12:g.107345122A= NCBI36
NG_008045.1:g.31301A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1215A= MANE Select ENSP00000205402.3:p.Ser405=
ENST00000205402.9:c.1215A= ENSP00000205402.3:p.Ser405=
ENST00000415325.5:c.*889A= ENSP00000402593.1:n.*889A=
ENST00000417551.5:c.1215A= ENSP00000390667.1:p.Ser405=
ENST00000437604.6:c.1071A= ENSP00000387542.2:p.Ser357=
ENST00000440410.5:c.1146A= ENSP00000417016.1:p.Ser382=
NM_000108.4:c.1215A= NP_000099.2:p.Ser405=
NM_001289750.1:c.918A= NP_001276679.1:p.Ser306=
NM_001289751.1:c.1146A= NP_001276680.1:p.Ser382=
NM_001289752.1:c.1071A= NP_001276681.1:p.Ser357=
NM_000108.5:c.1215A= MANE Select NP_000099.2:p.Ser405=