Canonical Allele Identifier: CA1105646314

Gene: DLD

Linked Data

• dbSNP Id: rs2032381322

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107920348del , CM000669.2:g.107920348del	GRCh38
NC_000007.13:g.107560793del , CM000669.1:g.107560793del	GRCh37
NC_000007.12:g.107348029del	NCBI36
NG_008045.1:g.34208del

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.*1089del MANE Select	ENSP00000205402.3:n.*1089del
ENST00000205402.9:c.*1089del	ENSP00000205402.3:n.*1089del
ENST00000417551.5:c.*124+965del	ENSP00000390667.1:n.*124+965del
NM_000108.4:c.*1089del	NP_000099.2:n.*1089del
NM_001289750.1:c.*1089del	NP_001276679.1:n.*1089del
NM_001289751.1:c.*1089del	NP_001276680.1:n.*1089del
NM_001289752.1:c.*1089del	NP_001276681.1:n.*1089del
NM_000108.5:c.*1089del MANE Select	NP_000099.2:n.*1089del