Canonical Allele Identifier: CA368857043
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915587G>T , CM000669.2:g.107915587G>T GRCh38
NC_000007.13:g.107556032G>T , CM000669.1:g.107556032G>T GRCh37
NC_000007.12:g.107343268G>T NCBI36
NG_008045.1:g.29447G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.766G>T MANE Select ENSP00000205402.3:p.Glu256Ter
ENST00000205402.9:c.766G>T ENSP00000205402.3:p.Glu256Ter
ENST00000415325.5:c.*440G>T ENSP00000402593.1:n.*440G>T
ENST00000417551.5:c.766G>T ENSP00000390667.1:p.Glu256Ter
ENST00000437604.6:c.622G>T ENSP00000387542.2:p.Glu208Ter
ENST00000440410.5:c.697G>T ENSP00000417016.1:p.Glu233Ter
ENST00000451081.5:c.*509G>T ENSP00000388077.1:n.*509G>T
NM_000108.4:c.766G>T NP_000099.2:p.Glu256Ter
NM_001289750.1:c.469G>T NP_001276679.1:p.Glu157Ter
NM_001289751.1:c.697G>T NP_001276680.1:p.Glu233Ter
NM_001289752.1:c.622G>T NP_001276681.1:p.Glu208Ter
NM_000108.5:c.766G>T MANE Select NP_000099.2:p.Glu256Ter