Canonical Allele Identifier: CA1732859337
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915594C= , CM000669.2:g.107915594C= GRCh38
NC_000007.13:g.107556039C= , CM000669.1:g.107556039C= GRCh37
NC_000007.12:g.107343275C= NCBI36
NG_008045.1:g.29454C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.773C= MANE Select ENSP00000205402.3:p.Ser258=
ENST00000205402.9:c.773C= ENSP00000205402.3:p.Ser258=
ENST00000415325.5:c.*447C= ENSP00000402593.1:n.*447C=
ENST00000417551.5:c.773C= ENSP00000390667.1:p.Ser258=
ENST00000437604.6:c.629C= ENSP00000387542.2:p.Ser210=
ENST00000440410.5:c.704C= ENSP00000417016.1:p.Ser235=
ENST00000451081.5:c.*516C= ENSP00000388077.1:n.*516C=
NM_000108.4:c.773C= NP_000099.2:p.Ser258=
NM_001289750.1:c.476C= NP_001276679.1:p.Ser159=
NM_001289751.1:c.704C= NP_001276680.1:p.Ser235=
NM_001289752.1:c.629C= NP_001276681.1:p.Ser210=
NM_000108.5:c.773C= MANE Select NP_000099.2:p.Ser258=