Canonical Allele Identifier: CA1732852106

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893239_107893240delinsCT , CM000669.2:g.107893239_107893240delinsCT	GRCh38
NC_000007.13:g.107533684_107533685delinsCT , CM000669.1:g.107533684_107533685delinsCT	GRCh37
NC_000007.12:g.107320920_107320921delinsCT	NCBI36
NG_008045.1:g.7099_7100delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.79_80delinsCT MANE Select	ENSP00000205402.3:p.Leu27=
ENST00000639772.1:c.79_80delinsCT	ENSP00000492159.1:p.Leu27=
ENST00000205402.9:c.79_80delinsCT	ENSP00000205402.3:p.Leu27=
ENST00000415325.5:c.79_80delinsCT	ENSP00000402593.1:p.Leu27=
ENST00000417551.5:c.79_80delinsCT	ENSP00000390667.1:p.Leu27=
ENST00000437604.6:c.79_80delinsCT	ENSP00000387542.2:p.Leu27=
ENST00000440410.5:c.79_80delinsCT	ENSP00000417016.1:p.Leu27=
ENST00000450038.5:c.79_80delinsCT	ENSP00000409590.1:p.Leu27=
ENST00000451081.5:c.79_80delinsCT	ENSP00000388077.1:p.Leu27=
ENST00000453354.5:n.144_145delinsCT
ENST00000460577.5:n.113_114delinsCT
ENST00000485066.1:n.168_169delinsCT
ENST00000494441.1:n.224_225delinsCT
NM_000108.4:c.79_80delinsCT	NP_000099.2:p.Leu27=
NM_001289750.1:c.-70_-69delinsCT	NP_001276679.1:n.-70_-69delinsCT
NM_001289751.1:c.79_80delinsCT	NP_001276680.1:p.Leu27=
NM_001289752.1:c.79_80delinsCT	NP_001276681.1:p.Leu27=
NM_000108.5:c.79_80delinsCT MANE Select	NP_000099.2:p.Leu27=