Canonical Allele Identifier: CA1732859198

Gene: DLD

Linked Data

• dbSNP Id: rs2032239558

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915293_107915295dup , CM000669.2:g.107915293_107915295dup	GRCh38
NC_000007.13:g.107555738_107555740dup , CM000669.1:g.107555738_107555740dup	GRCh37
NC_000007.12:g.107342974_107342976dup	NCBI36
NG_008045.1:g.29153_29155dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.685-213_685-211dup MANE Select	ENSP00000205402.3:n.685-213_685-211dup
ENST00000205402.9:c.685-213_685-211dup	ENSP00000205402.3:n.685-213_685-211dup
ENST00000415325.5:c.*359-213_*359-211dup	ENSP00000402593.1:n.*359-213_*359-211dup
ENST00000417551.5:c.685-213_685-211dup	ENSP00000390667.1:n.685-213_685-211dup
ENST00000437604.6:c.541-213_541-211dup	ENSP00000387542.2:n.541-213_541-211dup
ENST00000440410.5:c.616-213_616-211dup	ENSP00000417016.1:n.616-213_616-211dup
ENST00000451081.5:c.*428-213_*428-211dup	ENSP00000388077.1:n.*428-213_*428-211dup
NM_000108.4:c.685-213_685-211dup	NP_000099.2:n.685-213_685-211dup
NM_001289750.1:c.388-213_388-211dup	NP_001276679.1:n.388-213_388-211dup
NM_001289751.1:c.616-213_616-211dup	NP_001276680.1:n.616-213_616-211dup
NM_001289752.1:c.541-213_541-211dup	NP_001276681.1:n.541-213_541-211dup
NM_000108.5:c.685-213_685-211dup MANE Select	NP_000099.2:n.685-213_685-211dup