Canonical Allele Identifier: CA368858017
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917279T>G , CM000669.2:g.107917279T>G GRCh38
NC_000007.13:g.107557724T>G , CM000669.1:g.107557724T>G GRCh37
NC_000007.12:g.107344960T>G NCBI36
NG_008045.1:g.31139T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1053T>G MANE Select ENSP00000205402.3:p.Tyr351Ter
ENST00000205402.9:c.1053T>G ENSP00000205402.3:p.Tyr351Ter
ENST00000415325.5:c.*727T>G ENSP00000402593.1:n.*727T>G
ENST00000417551.5:c.1053T>G ENSP00000390667.1:p.Tyr351Ter
ENST00000437604.6:c.909T>G ENSP00000387542.2:p.Tyr303Ter
ENST00000440410.5:c.984T>G ENSP00000417016.1:p.Tyr328Ter
NM_000108.4:c.1053T>G NP_000099.2:p.Tyr351Ter
NM_001289750.1:c.756T>G NP_001276679.1:p.Tyr252Ter
NM_001289751.1:c.984T>G NP_001276680.1:p.Tyr328Ter
NM_001289752.1:c.909T>G NP_001276681.1:p.Tyr303Ter
NM_000108.5:c.1053T>G MANE Select NP_000099.2:p.Tyr351Ter