Canonical Allele Identifier: CA164262514

Gene: DLD

Linked Data

• dbSNP Id: rs751489107
• MyVariant Identifiers: chr7:g.107560896_107560899del (hg19) ; chr7:g.107920451_107920454del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107920455_107920458del , CM000669.2:g.107920455_107920458del	GRCh38
NC_000007.13:g.107560900_107560903del , CM000669.1:g.107560900_107560903del	GRCh37
NC_000007.12:g.107348136_107348139del	NCBI36
NG_008045.1:g.34315_34318del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*1196_*1199del MANE Select	ENSP00000205402.3:n.*1196_*1199del
ENST00000205402.9:c.*1196_*1199del	ENSP00000205402.3:n.*1196_*1199del
ENST00000417551.5:c.*124+1072_*124+1075del	ENSP00000390667.1:n.*124+1072_*124+1075del
NM_000108.4:c.*1196_*1199del	NP_000099.2:n.*1196_*1199del
NM_001289750.1:c.*1196_*1199del	NP_001276679.1:n.*1196_*1199del
NM_001289751.1:c.*1196_*1199del	NP_001276680.1:n.*1196_*1199del
NM_001289752.1:c.*1196_*1199del	NP_001276681.1:n.*1196_*1199del
NM_000108.5:c.*1196_*1199del MANE Select	NP_000099.2:n.*1196_*1199del