Canonical Allele Identifier: CA2777360531
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107893282_107893283insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA , CM000669.2:g.107893282_107893283insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA GRCh38
NC_000007.13:g.107533727_107533728insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA , CM000669.1:g.107533727_107533728insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA GRCh37
NC_000007.12:g.107320963_107320964insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA NCBI36
NG_008045.1:g.7142_7143insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA MANE Select ENSP00000205402.3:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGAT...
ENST00000639772.1:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA ENSP00000492159.1:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGAT...
ENST00000205402.9:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA ENSP00000205402.3:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGAT...
ENST00000415325.5:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA ENSP00000402593.1:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGAT...
ENST00000417551.5:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA ENSP00000390667.1:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGAT...
ENST00000437604.6:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA ENSP00000387542.2:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGAT...
ENST00000440410.5:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA ENSP00000417016.1:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGAT...
ENST00000450038.5:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA ENSP00000409590.1:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGAT...
ENST00000451081.5:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA ENSP00000388077.1:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGAT...
ENST00000453354.5:n.183+4_183+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA
ENST00000460577.5:n.152+4_152+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA
ENST00000485066.1:n.211_212insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA
ENST00000494441.1:n.263+4_263+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA
NM_000108.4:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA NP_000099.2:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTG...
NM_001289750.1:c.-31+4_-31+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA NP_001276679.1:n.-31+4_-31+5insCAGTTATAGGTTCTGGTCCTGGAGGATATG...
NM_001289751.1:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA NP_001276680.1:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATG...
NM_001289752.1:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA NP_001276681.1:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATG...
NM_000108.5:c.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTGCTGCTATTAAA MANE Select NP_000099.2:n.118+4_118+5insCAGTTATAGGTTCTGGTCCTGGAGGATATGTTG...