Canonical Allele Identifier: CA1732859164

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915210_107915211delinsCT , CM000669.2:g.107915210_107915211delinsCT	GRCh38
NC_000007.13:g.107555655_107555656delinsCT , CM000669.1:g.107555655_107555656delinsCT	GRCh37
NC_000007.12:g.107342891_107342892delinsCT	NCBI36
NG_008045.1:g.29070_29071delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.685-296_685-295delinsCT MANE Select	ENSP00000205402.3:n.685-296_685-295delinsCT
ENST00000205402.9:c.685-296_685-295delinsCT	ENSP00000205402.3:n.685-296_685-295delinsCT
ENST00000415325.5:c.*359-296_*359-295delinsCT	ENSP00000402593.1:n.*359-296_*359-295delinsCT
ENST00000417551.5:c.685-296_685-295delinsCT	ENSP00000390667.1:n.685-296_685-295delinsCT
ENST00000437604.6:c.541-296_541-295delinsCT	ENSP00000387542.2:n.541-296_541-295delinsCT
ENST00000440410.5:c.616-296_616-295delinsCT	ENSP00000417016.1:n.616-296_616-295delinsCT
ENST00000451081.5:c.*428-296_*428-295delinsCT	ENSP00000388077.1:n.*428-296_*428-295delinsCT
NM_000108.4:c.685-296_685-295delinsCT	NP_000099.2:n.685-296_685-295delinsCT
NM_001289750.1:c.388-296_388-295delinsCT	NP_001276679.1:n.388-296_388-295delinsCT
NM_001289751.1:c.616-296_616-295delinsCT	NP_001276680.1:n.616-296_616-295delinsCT
NM_001289752.1:c.541-296_541-295delinsCT	NP_001276681.1:n.541-296_541-295delinsCT
NM_000108.5:c.685-296_685-295delinsCT MANE Select	NP_000099.2:n.685-296_685-295delinsCT