Canonical Allele Identifier: CA2777360529
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107893278_107893279insTTGATGCTGAT , CM000669.2:g.107893278_107893279insTTGATGCTGAT GRCh38
NC_000007.13:g.107533723_107533724insTTGATGCTGAT , CM000669.1:g.107533723_107533724insTTGATGCTGAT GRCh37
NC_000007.12:g.107320959_107320960insTTGATGCTGAT NCBI36
NG_008045.1:g.7138_7139insTTGATGCTGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.118_118+1insTTGATGCTGAT MANE Select ENSP00000205402.3:n.118_118+1insTTGATGCTGAT
ENST00000639772.1:c.118_118+1insTTGATGCTGAT ENSP00000492159.1:n.118_118+1insTTGATGCTGAT
ENST00000205402.9:c.118_118+1insTTGATGCTGAT ENSP00000205402.3:n.118_118+1insTTGATGCTGAT
ENST00000415325.5:c.118_118+1insTTGATGCTGAT ENSP00000402593.1:n.118_118+1insTTGATGCTGAT
ENST00000417551.5:c.118_118+1insTTGATGCTGAT ENSP00000390667.1:n.118_118+1insTTGATGCTGAT
ENST00000437604.6:c.118_118+1insTTGATGCTGAT ENSP00000387542.2:n.118_118+1insTTGATGCTGAT
ENST00000440410.5:c.118_118+1insTTGATGCTGAT ENSP00000417016.1:n.118_118+1insTTGATGCTGAT
ENST00000450038.5:c.118_118+1insTTGATGCTGAT ENSP00000409590.1:n.118_118+1insTTGATGCTGAT
ENST00000451081.5:c.118_118+1insTTGATGCTGAT ENSP00000388077.1:n.118_118+1insTTGATGCTGAT
ENST00000453354.5:n.183_183+1insTTGATGCTGAT
ENST00000460577.5:n.152_152+1insTTGATGCTGAT
ENST00000485066.1:n.207_208insTTGATGCTGAT
ENST00000494441.1:n.263_263+1insTTGATGCTGAT
NM_000108.4:c.118_118+1insTTGATGCTGAT NP_000099.2:n.118_118+1insTTGATGCTGAT
NM_001289750.1:c.-31_-31+1insTTGATGCTGAT NP_001276679.1:n.-31_-31+1insTTGATGCTGAT
NM_001289751.1:c.118_118+1insTTGATGCTGAT NP_001276680.1:n.118_118+1insTTGATGCTGAT
NM_001289752.1:c.118_118+1insTTGATGCTGAT NP_001276681.1:n.118_118+1insTTGATGCTGAT
NM_000108.5:c.118_118+1insTTGATGCTGAT MANE Select NP_000099.2:n.118_118+1insTTGATGCTGAT