Canonical Allele Identifier: CA1732860735

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919063_107919067delinsCTGTG , CM000669.2:g.107919063_107919067delinsCTGTG	GRCh38
NC_000007.13:g.107559508_107559512delinsCTGTG , CM000669.1:g.107559508_107559512delinsCTGTG	GRCh37
NC_000007.12:g.107346744_107346748delinsCTGTG	NCBI36
NG_008045.1:g.32923_32927delinsCTGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1428_1432delinsCTGTG MANE Select	ENSP00000205402.3:p.Ser476=
ENST00000205402.9:c.1428_1432delinsCTGTG	ENSP00000205402.3:p.Ser476=
ENST00000415325.5:c.*1102_*1106delinsCTGTG	ENSP00000402593.1:n.*1102_*1106delinsCTGTG
ENST00000417551.5:c.1428_1432delinsCTGTG	ENSP00000390667.1:p.Ser476=
ENST00000437604.6:c.1284_1288delinsCTGTG	ENSP00000387542.2:p.Ser428=
ENST00000440410.5:c.1359_1363delinsCTGTG	ENSP00000417016.1:p.Ser453=
NM_000108.4:c.1428_1432delinsCTGTG	NP_000099.2:p.Ser476=
NM_001289750.1:c.1131_1135delinsCTGTG	NP_001276679.1:p.Ser377=
NM_001289751.1:c.1359_1363delinsCTGTG	NP_001276680.1:p.Ser453=
NM_001289752.1:c.1284_1288delinsCTGTG	NP_001276681.1:p.Ser428=
NM_000108.5:c.1428_1432delinsCTGTG MANE Select	NP_000099.2:p.Ser476=