Canonical Allele Identifier: CA1105646056

Gene: DLD

Linked Data

• dbSNP Id: rs2032367664
• gnomAD v3: 7-107919926-T-TG
• gnomAD v4: 7-107919926-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919930dup , CM000669.2:g.107919930dup	GRCh38
NC_000007.13:g.107560375dup , CM000669.1:g.107560375dup	GRCh37
NC_000007.12:g.107347611dup	NCBI36
NG_008045.1:g.33790dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*671dup MANE Select	ENSP00000205402.3:n.*671dup
ENST00000205402.9:c.*671dup	ENSP00000205402.3:n.*671dup
ENST00000417551.5:c.*124+547dup	ENSP00000390667.1:n.*124+547dup
NM_000108.4:c.*671dup	NP_000099.2:n.*671dup
NM_001289750.1:c.*671dup	NP_001276679.1:n.*671dup
NM_001289751.1:c.*671dup	NP_001276680.1:n.*671dup
NM_001289752.1:c.*671dup	NP_001276681.1:n.*671dup
NM_000108.5:c.*671dup MANE Select	NP_000099.2:n.*671dup