Canonical Allele Identifier: CA1732859284
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915475T= , CM000669.2:g.107915475T= GRCh38
NC_000007.13:g.107555920T= , CM000669.1:g.107555920T= GRCh37
NC_000007.12:g.107343156T= NCBI36
NG_008045.1:g.29335T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.685-31T= MANE Select ENSP00000205402.3:n.685-31T=
ENST00000205402.9:c.685-31T= ENSP00000205402.3:n.685-31T=
ENST00000415325.5:c.*359-31T= ENSP00000402593.1:n.*359-31T=
ENST00000417551.5:c.685-31T= ENSP00000390667.1:n.685-31T=
ENST00000437604.6:c.541-31T= ENSP00000387542.2:n.541-31T=
ENST00000440410.5:c.616-31T= ENSP00000417016.1:n.616-31T=
ENST00000451081.5:c.*428-31T= ENSP00000388077.1:n.*428-31T=
NM_000108.4:c.685-31T= NP_000099.2:n.685-31T=
NM_001289750.1:c.388-31T= NP_001276679.1:n.388-31T=
NM_001289751.1:c.616-31T= NP_001276680.1:n.616-31T=
NM_001289752.1:c.541-31T= NP_001276681.1:n.541-31T=
NM_000108.5:c.685-31T= MANE Select NP_000099.2:n.685-31T=