Canonical Allele Identifier: CA1732848985
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107901703_107901704delinsAT , CM000669.2:g.107901703_107901704delinsAT GRCh38
NC_000007.13:g.107542148_107542149delinsAT , CM000669.1:g.107542148_107542149delinsAT GRCh37
NC_000007.12:g.107329384_107329385delinsAT NCBI36
NG_008045.1:g.15563_15564delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.119-35_119-34delinsAT MANE Select ENSP00000205402.3:n.119-35_119-34delinsAT
ENST00000639772.1:c.119-35_119-34delinsAT ENSP00000492159.1:n.119-35_119-34delinsAT
ENST00000205402.9:c.119-35_119-34delinsAT ENSP00000205402.3:n.119-35_119-34delinsAT
ENST00000415325.5:c.119-1775_119-1774delinsAT ENSP00000402593.1:n.119-1775_119-1774delinsAT
ENST00000417551.5:c.119-35_119-34delinsAT ENSP00000390667.1:n.119-35_119-34delinsAT
ENST00000437604.6:c.119-35_119-34delinsAT ENSP00000387542.2:n.119-35_119-34delinsAT
ENST00000440410.5:c.119-35_119-34delinsAT ENSP00000417016.1:n.119-35_119-34delinsAT
ENST00000450038.5:c.119-35_119-34delinsAT ENSP00000409590.1:n.119-35_119-34delinsAT
ENST00000451081.5:c.119-35_119-34delinsAT ENSP00000388077.1:n.119-35_119-34delinsAT
ENST00000453354.5:n.184-35_184-34delinsAT
ENST00000460577.5:n.153-35_153-34delinsAT
ENST00000494441.1:n.264-35_264-34delinsAT
NM_000108.4:c.119-35_119-34delinsAT NP_000099.2:n.119-35_119-34delinsAT
NM_001289750.1:c.-30-1775_-30-1774delinsAT NP_001276679.1:n.-30-1775_-30-1774delinsAT
NM_001289751.1:c.119-35_119-34delinsAT NP_001276680.1:n.119-35_119-34delinsAT
NM_001289752.1:c.119-35_119-34delinsAT NP_001276681.1:n.119-35_119-34delinsAT
NM_000108.5:c.119-35_119-34delinsAT MANE Select NP_000099.2:n.119-35_119-34delinsAT