Canonical Allele Identifier: CA1732859360
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915647A= , CM000669.2:g.107915647A= GRCh38
NC_000007.13:g.107556092A= , CM000669.1:g.107556092A= GRCh37
NC_000007.12:g.107343328A= NCBI36
NG_008045.1:g.29507A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.826A= MANE Select ENSP00000205402.3:p.Thr276=
ENST00000205402.9:c.826A= ENSP00000205402.3:p.Thr276=
ENST00000415325.5:c.*500A= ENSP00000402593.1:n.*500A=
ENST00000417551.5:c.826A= ENSP00000390667.1:p.Thr276=
ENST00000437604.6:c.682A= ENSP00000387542.2:p.Thr228=
ENST00000440410.5:c.757A= ENSP00000417016.1:p.Thr253=
NM_000108.4:c.826A= NP_000099.2:p.Thr276=
NM_001289750.1:c.529A= NP_001276679.1:p.Thr177=
NM_001289751.1:c.757A= NP_001276680.1:p.Thr253=
NM_001289752.1:c.682A= NP_001276681.1:p.Thr228=
NM_000108.5:c.826A= MANE Select NP_000099.2:p.Thr276=