Canonical Allele Identifier: CA1105646280
Gene: DLD HGNC NCBI

Linked Data

gnomAD v3: 7-107920285-C-CTCT
gnomAD v4: 7-107920285-C-CTCT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920286_107920287insCTT , CM000669.2:g.107920286_107920287insCTT GRCh38
NC_000007.13:g.107560731_107560732insCTT , CM000669.1:g.107560731_107560732insCTT GRCh37
NC_000007.12:g.107347967_107347968insCTT NCBI36
NG_008045.1:g.34146_34147insCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*1027_*1028insCTT MANE Select ENSP00000205402.3:n.*1027_*1028insCTT
ENST00000205402.9:c.*1027_*1028insCTT ENSP00000205402.3:n.*1027_*1028insCTT
ENST00000417551.5:c.*124+903_*124+904insCTT ENSP00000390667.1:n.*124+903_*124+904insCTT
NM_000108.4:c.*1027_*1028insCTT NP_000099.2:n.*1027_*1028insCTT
NM_001289750.1:c.*1027_*1028insCTT NP_001276679.1:n.*1027_*1028insCTT
NM_001289751.1:c.*1027_*1028insCTT NP_001276680.1:n.*1027_*1028insCTT
NM_001289752.1:c.*1027_*1028insCTT NP_001276681.1:n.*1027_*1028insCTT
NM_000108.5:c.*1027_*1028insCTT MANE Select NP_000099.2:n.*1027_*1028insCTT
Search 100 bp 5'
Search 100 bp 3'