Canonical Allele Identifier: CA1732861122
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919975_107919978delinsTATC , CM000669.2:g.107919975_107919978delinsTATC GRCh38
NC_000007.13:g.107560420_107560423delinsTATC , CM000669.1:g.107560420_107560423delinsTATC GRCh37
NC_000007.12:g.107347656_107347659delinsTATC NCBI36
NG_008045.1:g.33835_33838delinsTATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*716_*719delinsTATC MANE Select ENSP00000205402.3:n.*716_*719delinsTATC
ENST00000205402.9:c.*716_*719delinsTATC ENSP00000205402.3:n.*716_*719delinsTATC
ENST00000417551.5:c.*124+592_*124+595delinsTATC ENSP00000390667.1:n.*124+592_*124+595delinsTATC
NM_000108.4:c.*716_*719delinsTATC NP_000099.2:n.*716_*719delinsTATC
NM_001289750.1:c.*716_*719delinsTATC NP_001276679.1:n.*716_*719delinsTATC
NM_001289751.1:c.*716_*719delinsTATC NP_001276680.1:n.*716_*719delinsTATC
NM_001289752.1:c.*716_*719delinsTATC NP_001276681.1:n.*716_*719delinsTATC
NM_000108.5:c.*716_*719delinsTATC MANE Select NP_000099.2:n.*716_*719delinsTATC