Canonical Allele Identifier: CA1732861149
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920022T= , CM000669.2:g.107920022T= GRCh38
NC_000007.13:g.107560467T= , CM000669.1:g.107560467T= GRCh37
NC_000007.12:g.107347703T= NCBI36
NG_008045.1:g.33882T=

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*763T= MANE Select ENSP00000205402.3:n.*763T=
ENST00000205402.9:c.*763T= ENSP00000205402.3:n.*763T=
ENST00000417551.5:c.*124+639T= ENSP00000390667.1:n.*124+639T=
NM_000108.4:c.*763T= NP_000099.2:n.*763T=
NM_001289750.1:c.*763T= NP_001276679.1:n.*763T=
NM_001289751.1:c.*763T= NP_001276680.1:n.*763T=
NM_001289752.1:c.*763T= NP_001276681.1:n.*763T=
NM_000108.5:c.*763T= MANE Select NP_000099.2:n.*763T=