Canonical Allele Identifier: CA1732860075
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917439T= , CM000669.2:g.107917439T= GRCh38
NC_000007.13:g.107557884T= , CM000669.1:g.107557884T= GRCh37
NC_000007.12:g.107345120T= NCBI36
NG_008045.1:g.31299T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1213T= MANE Select ENSP00000205402.3:p.Ser405=
ENST00000205402.9:c.1213T= ENSP00000205402.3:p.Ser405=
ENST00000415325.5:c.*887T= ENSP00000402593.1:n.*887T=
ENST00000417551.5:c.1213T= ENSP00000390667.1:p.Ser405=
ENST00000437604.6:c.1069T= ENSP00000387542.2:p.Ser357=
ENST00000440410.5:c.1144T= ENSP00000417016.1:p.Ser382=
NM_000108.4:c.1213T= NP_000099.2:p.Ser405=
NM_001289750.1:c.916T= NP_001276679.1:p.Ser306=
NM_001289751.1:c.1144T= NP_001276680.1:p.Ser382=
NM_001289752.1:c.1069T= NP_001276681.1:p.Ser357=
NM_000108.5:c.1213T= MANE Select NP_000099.2:p.Ser405=