Canonical Allele Identifier: CA1732859306
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915506G= , CM000669.2:g.107915506G= GRCh38
NC_000007.13:g.107555951G= , CM000669.1:g.107555951G= GRCh37
NC_000007.12:g.107343187G= NCBI36
NG_008045.1:g.29366G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.685G= MANE Select ENSP00000205402.3:p.Gly229=
ENST00000205402.9:c.685G= ENSP00000205402.3:p.Gly229=
ENST00000415325.5:c.*359G= ENSP00000402593.1:n.*359G=
ENST00000417551.5:c.685G= ENSP00000390667.1:p.Gly229=
ENST00000437604.6:c.541G= ENSP00000387542.2:p.Gly181=
ENST00000440410.5:c.616G= ENSP00000417016.1:p.Gly206=
ENST00000451081.5:c.*428G= ENSP00000388077.1:n.*428G=
NM_000108.4:c.685G= NP_000099.2:p.Gly229=
NM_001289750.1:c.388G= NP_001276679.1:p.Gly130=
NM_001289751.1:c.616G= NP_001276680.1:p.Gly206=
NM_001289752.1:c.541G= NP_001276681.1:p.Gly181=
NM_000108.5:c.685G= MANE Select NP_000099.2:p.Gly229=