Canonical Allele Identifier: CA1105646079

Gene: DLD

Linked Data

• dbSNP Id: rs1695249004
• gnomAD v3: 7-107920035-C-CT
• gnomAD v4: 7-107920035-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107920036dup , CM000669.2:g.107920036dup	GRCh38
NC_000007.13:g.107560481dup , CM000669.1:g.107560481dup	GRCh37
NC_000007.12:g.107347717dup	NCBI36
NG_008045.1:g.33896dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*777dup MANE Select	ENSP00000205402.3:n.*777dup
ENST00000205402.9:c.*777dup	ENSP00000205402.3:n.*777dup
ENST00000417551.5:c.*124+653dup	ENSP00000390667.1:n.*124+653dup
NM_000108.4:c.*777dup	NP_000099.2:n.*777dup
NM_001289750.1:c.*777dup	NP_001276679.1:n.*777dup
NM_001289751.1:c.*777dup	NP_001276680.1:n.*777dup
NM_001289752.1:c.*777dup	NP_001276681.1:n.*777dup
NM_000108.5:c.*777dup MANE Select	NP_000099.2:n.*777dup