Canonical Allele Identifier: CA1732859323
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915561A= , CM000669.2:g.107915561A= GRCh38
NC_000007.13:g.107556006A= , CM000669.1:g.107556006A= GRCh37
NC_000007.12:g.107343242A= NCBI36
NG_008045.1:g.29421A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.740A= MANE Select ENSP00000205402.3:p.His247=
ENST00000205402.9:c.740A= ENSP00000205402.3:p.His247=
ENST00000415325.5:c.*414A= ENSP00000402593.1:n.*414A=
ENST00000417551.5:c.740A= ENSP00000390667.1:p.His247=
ENST00000437604.6:c.596A= ENSP00000387542.2:p.His199=
ENST00000440410.5:c.671A= ENSP00000417016.1:p.His224=
ENST00000451081.5:c.*483A= ENSP00000388077.1:n.*483A=
NM_000108.4:c.740A= NP_000099.2:p.His247=
NM_001289750.1:c.443A= NP_001276679.1:p.His148=
NM_001289751.1:c.671A= NP_001276680.1:p.His224=
NM_001289752.1:c.596A= NP_001276681.1:p.His199=
NM_000108.5:c.740A= MANE Select NP_000099.2:p.His247=