Canonical Allele Identifier: CA1732861236
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920202C= , CM000669.2:g.107920202C= GRCh38
NC_000007.13:g.107560647C= , CM000669.1:g.107560647C= GRCh37
NC_000007.12:g.107347883C= NCBI36
NG_008045.1:g.34062C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*943C= MANE Select ENSP00000205402.3:n.*943C=
ENST00000205402.9:c.*943C= ENSP00000205402.3:n.*943C=
ENST00000417551.5:c.*124+819C= ENSP00000390667.1:n.*124+819C=
NM_000108.4:c.*943C= NP_000099.2:n.*943C=
NM_001289750.1:c.*943C= NP_001276679.1:n.*943C=
NM_001289751.1:c.*943C= NP_001276680.1:n.*943C=
NM_001289752.1:c.*943C= NP_001276681.1:n.*943C=
NM_000108.5:c.*943C= MANE Select NP_000099.2:n.*943C=