Canonical Allele Identifier: CA2684458338

Gene: DLD

Linked Data

• gnomAD v4: 7-107916953-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916957del , CM000669.2:g.107916957del	GRCh38
NC_000007.13:g.107557402del , CM000669.1:g.107557402del	GRCh37
NC_000007.12:g.107344638del	NCBI36
NG_008045.1:g.30817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1039del MANE Select	ENSP00000205402.3:p.Ile347PhefsTer10
ENST00000205402.9:c.1039del	ENSP00000205402.3:p.Ile347PhefsTer10
ENST00000415325.5:c.*713del	ENSP00000402593.1:n.*713del
ENST00000417551.5:c.1039del	ENSP00000390667.1:p.Ile347PhefsTer10
ENST00000437604.6:c.895del	ENSP00000387542.2:p.Ile299PhefsTer10
ENST00000440410.5:c.970del	ENSP00000417016.1:p.Ile324PhefsTer10
NM_000108.4:c.1039del	NP_000099.2:p.Ile347PhefsTer10
NM_001289750.1:c.742del	NP_001276679.1:p.Ile248PhefsTer10
NM_001289751.1:c.970del	NP_001276680.1:p.Ile324PhefsTer10
NM_001289752.1:c.895del	NP_001276681.1:p.Ile299PhefsTer10
NM_000108.5:c.1039del MANE Select	NP_000099.2:p.Ile347PhefsTer10