Canonical Allele Identifier: CA1732859240
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915392T= , CM000669.2:g.107915392T= GRCh38
NC_000007.13:g.107555837T= , CM000669.1:g.107555837T= GRCh37
NC_000007.12:g.107343073T= NCBI36
NG_008045.1:g.29252T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.685-114T= MANE Select ENSP00000205402.3:n.685-114T=
ENST00000205402.9:c.685-114T= ENSP00000205402.3:n.685-114T=
ENST00000415325.5:c.*359-114T= ENSP00000402593.1:n.*359-114T=
ENST00000417551.5:c.685-114T= ENSP00000390667.1:n.685-114T=
ENST00000437604.6:c.541-114T= ENSP00000387542.2:n.541-114T=
ENST00000440410.5:c.616-114T= ENSP00000417016.1:n.616-114T=
ENST00000451081.5:c.*428-114T= ENSP00000388077.1:n.*428-114T=
NM_000108.4:c.685-114T= NP_000099.2:n.685-114T=
NM_001289750.1:c.388-114T= NP_001276679.1:n.388-114T=
NM_001289751.1:c.616-114T= NP_001276680.1:n.616-114T=
NM_001289752.1:c.541-114T= NP_001276681.1:n.541-114T=
NM_000108.5:c.685-114T= MANE Select NP_000099.2:n.685-114T=