Canonical Allele Identifier: CA1732860827
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919263A= , CM000669.2:g.107919263A= GRCh38
NC_000007.13:g.107559708A= , CM000669.1:g.107559708A= GRCh37
NC_000007.12:g.107346944A= NCBI36
NG_008045.1:g.33123A=

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*4A= MANE Select ENSP00000205402.3:n.*4A=
ENST00000205402.9:c.*4A= ENSP00000205402.3:n.*4A=
ENST00000415325.5:c.*1208A= ENSP00000402593.1:n.*1208A=
ENST00000417551.5:c.*4A= ENSP00000390667.1:n.*4A=
ENST00000437604.6:c.*4A= ENSP00000387542.2:n.*4A=
ENST00000440410.5:c.*4A= ENSP00000417016.1:n.*4A=
NM_000108.4:c.*4A= NP_000099.2:n.*4A=
NM_001289750.1:c.*4A= NP_001276679.1:n.*4A=
NM_001289751.1:c.*4A= NP_001276680.1:n.*4A=
NM_001289752.1:c.*4A= NP_001276681.1:n.*4A=
NM_000108.5:c.*4A= MANE Select NP_000099.2:n.*4A=