Canonical Allele Identifier: CA1732859384
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915697G= , CM000669.2:g.107915697G= GRCh38
NC_000007.13:g.107556142G= , CM000669.1:g.107556142G= GRCh37
NC_000007.12:g.107343378G= NCBI36
NG_008045.1:g.29557G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.875+1G= MANE Select ENSP00000205402.3:n.875+1G=
ENST00000205402.9:c.875+1G= ENSP00000205402.3:n.875+1G=
ENST00000415325.5:c.*549+1G= ENSP00000402593.1:n.*549+1G=
ENST00000417551.5:c.875+1G= ENSP00000390667.1:n.875+1G=
ENST00000437604.6:c.731+1G= ENSP00000387542.2:n.731+1G=
ENST00000440410.5:c.806+1G= ENSP00000417016.1:n.806+1G=
NM_000108.4:c.875+1G= NP_000099.2:n.875+1G=
NM_001289750.1:c.578+1G= NP_001276679.1:n.578+1G=
NM_001289751.1:c.806+1G= NP_001276680.1:n.806+1G=
NM_001289752.1:c.731+1G= NP_001276681.1:n.731+1G=
NM_000108.5:c.875+1G= MANE Select NP_000099.2:n.875+1G=