Canonical Allele Identifier: CA1732859315
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915541A= , CM000669.2:g.107915541A= GRCh38
NC_000007.13:g.107555986A= , CM000669.1:g.107555986A= GRCh37
NC_000007.12:g.107343222A= NCBI36
NG_008045.1:g.29401A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.720A= MANE Select ENSP00000205402.3:p.Thr240=
ENST00000205402.9:c.720A= ENSP00000205402.3:p.Thr240=
ENST00000415325.5:c.*394A= ENSP00000402593.1:n.*394A=
ENST00000417551.5:c.720A= ENSP00000390667.1:p.Thr240=
ENST00000437604.6:c.576A= ENSP00000387542.2:p.Thr192=
ENST00000440410.5:c.651A= ENSP00000417016.1:p.Thr217=
ENST00000451081.5:c.*463A= ENSP00000388077.1:n.*463A=
NM_000108.4:c.720A= NP_000099.2:p.Thr240=
NM_001289750.1:c.423A= NP_001276679.1:p.Thr141=
NM_001289751.1:c.651A= NP_001276680.1:p.Thr217=
NM_001289752.1:c.576A= NP_001276681.1:p.Thr192=
NM_000108.5:c.720A= MANE Select NP_000099.2:p.Thr240=