Canonical Allele Identifier: CA1732861263
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920252_107920255delinsTGTG , CM000669.2:g.107920252_107920255delinsTGTG GRCh38
NC_000007.13:g.107560697_107560700delinsTGTG , CM000669.1:g.107560697_107560700delinsTGTG GRCh37
NC_000007.12:g.107347933_107347936delinsTGTG NCBI36
NG_008045.1:g.34112_34115delinsTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*993_*996delinsTGTG MANE Select ENSP00000205402.3:n.*993_*996delinsTGTG
ENST00000205402.9:c.*993_*996delinsTGTG ENSP00000205402.3:n.*993_*996delinsTGTG
ENST00000417551.5:c.*124+869_*124+872delinsTGTG ENSP00000390667.1:n.*124+869_*124+872delinsTGTG
NM_000108.4:c.*993_*996delinsTGTG NP_000099.2:n.*993_*996delinsTGTG
NM_001289750.1:c.*993_*996delinsTGTG NP_001276679.1:n.*993_*996delinsTGTG
NM_001289751.1:c.*993_*996delinsTGTG NP_001276680.1:n.*993_*996delinsTGTG
NM_001289752.1:c.*993_*996delinsTGTG NP_001276681.1:n.*993_*996delinsTGTG
NM_000108.5:c.*993_*996delinsTGTG MANE Select NP_000099.2:n.*993_*996delinsTGTG