Canonical Allele Identifier: CA1732861332
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs1038410210
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920381A>G , CM000669.2:g.107920381A>G GRCh38
NC_000007.13:g.107560826A>G , CM000669.1:g.107560826A>G GRCh37
NC_000007.12:g.107348062A>G NCBI36
NG_008045.1:g.34241A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*1122A>G MANE Select ENSP00000205402.3:n.*1122A>G
ENST00000205402.9:c.*1122A>G ENSP00000205402.3:n.*1122A>G
ENST00000417551.5:c.*124+998A>G ENSP00000390667.1:n.*124+998A>G
NM_000108.4:c.*1122A>G NP_000099.2:n.*1122A>G
NM_001289750.1:c.*1122A>G NP_001276679.1:n.*1122A>G
NM_001289751.1:c.*1122A>G NP_001276680.1:n.*1122A>G
NM_001289752.1:c.*1122A>G NP_001276681.1:n.*1122A>G
NM_000108.5:c.*1122A>G MANE Select NP_000099.2:n.*1122A>G
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