Canonical Allele Identifier: CA1732860715
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919017G= , CM000669.2:g.107919017G= GRCh38
NC_000007.13:g.107559462G= , CM000669.1:g.107559462G= GRCh37
NC_000007.12:g.107346698G= NCBI36
NG_008045.1:g.32877G=

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.1382G= MANE Select ENSP00000205402.3:p.Gly461=
ENST00000205402.9:c.1382G= ENSP00000205402.3:p.Gly461=
ENST00000415325.5:c.*1056G= ENSP00000402593.1:n.*1056G=
ENST00000417551.5:c.1382G= ENSP00000390667.1:p.Gly461=
ENST00000437604.6:c.1238G= ENSP00000387542.2:p.Gly413=
ENST00000440410.5:c.1313G= ENSP00000417016.1:p.Gly438=
NM_000108.4:c.1382G= NP_000099.2:p.Gly461=
NM_001289750.1:c.1085G= NP_001276679.1:p.Gly362=
NM_001289751.1:c.1313G= NP_001276680.1:p.Gly438=
NM_001289752.1:c.1238G= NP_001276681.1:p.Gly413=
NM_000108.5:c.1382G= MANE Select NP_000099.2:p.Gly461=