Canonical Allele Identifier: CA1732848990
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107901708_107901713delinsCTATTT , CM000669.2:g.107901708_107901713delinsCTATTT GRCh38
NC_000007.13:g.107542153_107542158delinsCTATTT , CM000669.1:g.107542153_107542158delinsCTATTT GRCh37
NC_000007.12:g.107329389_107329394delinsCTATTT NCBI36
NG_008045.1:g.15568_15573delinsCTATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.119-30_119-25delinsCTATTT MANE Select ENSP00000205402.3:n.119-30_119-25delinsCTATTT
ENST00000639772.1:c.119-30_119-25delinsCTATTT ENSP00000492159.1:n.119-30_119-25delinsCTATTT
ENST00000205402.9:c.119-30_119-25delinsCTATTT ENSP00000205402.3:n.119-30_119-25delinsCTATTT
ENST00000415325.5:c.119-1770_119-1765delinsCTATTT ENSP00000402593.1:n.119-1770_119-1765delinsCTATTT
ENST00000417551.5:c.119-30_119-25delinsCTATTT ENSP00000390667.1:n.119-30_119-25delinsCTATTT
ENST00000437604.6:c.119-30_119-25delinsCTATTT ENSP00000387542.2:n.119-30_119-25delinsCTATTT
ENST00000440410.5:c.119-30_119-25delinsCTATTT ENSP00000417016.1:n.119-30_119-25delinsCTATTT
ENST00000450038.5:c.119-30_119-25delinsCTATTT ENSP00000409590.1:n.119-30_119-25delinsCTATTT
ENST00000451081.5:c.119-30_119-25delinsCTATTT ENSP00000388077.1:n.119-30_119-25delinsCTATTT
ENST00000453354.5:n.184-30_184-25delinsCTATTT
ENST00000460577.5:n.153-30_153-25delinsCTATTT
ENST00000494441.1:n.264-30_264-25delinsCTATTT
NM_000108.4:c.119-30_119-25delinsCTATTT NP_000099.2:n.119-30_119-25delinsCTATTT
NM_001289750.1:c.-30-1770_-30-1765delinsCTATTT NP_001276679.1:n.-30-1770_-30-1765delinsCTATTT
NM_001289751.1:c.119-30_119-25delinsCTATTT NP_001276680.1:n.119-30_119-25delinsCTATTT
NM_001289752.1:c.119-30_119-25delinsCTATTT NP_001276681.1:n.119-30_119-25delinsCTATTT
NM_000108.5:c.119-30_119-25delinsCTATTT MANE Select NP_000099.2:n.119-30_119-25delinsCTATTT