Canonical Allele Identifier: CA1732861208
Gene: DLD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920151T= , CM000669.2:g.107920151T= GRCh38
NC_000007.13:g.107560596T= , CM000669.1:g.107560596T= GRCh37
NC_000007.12:g.107347832T= NCBI36
NG_008045.1:g.34011T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*892T= MANE Select ENSP00000205402.3:n.*892T=
ENST00000205402.9:c.*892T= ENSP00000205402.3:n.*892T=
ENST00000417551.5:c.*124+768T= ENSP00000390667.1:n.*124+768T=
NM_000108.4:c.*892T= NP_000099.2:n.*892T=
NM_001289750.1:c.*892T= NP_001276679.1:n.*892T=
NM_001289751.1:c.*892T= NP_001276680.1:n.*892T=
NM_001289752.1:c.*892T= NP_001276681.1:n.*892T=
NM_000108.5:c.*892T= MANE Select NP_000099.2:n.*892T=
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