Canonical Allele Identifier: CA1732861331
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920381A= , CM000669.2:g.107920381A= GRCh38
NC_000007.13:g.107560826A= , CM000669.1:g.107560826A= GRCh37
NC_000007.12:g.107348062A= NCBI36
NG_008045.1:g.34241A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*1122A= MANE Select ENSP00000205402.3:n.*1122A=
ENST00000205402.9:c.*1122A= ENSP00000205402.3:n.*1122A=
ENST00000417551.5:c.*124+998A= ENSP00000390667.1:n.*124+998A=
NM_000108.4:c.*1122A= NP_000099.2:n.*1122A=
NM_001289750.1:c.*1122A= NP_001276679.1:n.*1122A=
NM_001289751.1:c.*1122A= NP_001276680.1:n.*1122A=
NM_001289752.1:c.*1122A= NP_001276681.1:n.*1122A=
NM_000108.5:c.*1122A= MANE Select NP_000099.2:n.*1122A=