Canonical Allele Identifier: CA1732861147
Gene: DLD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920019_107920022delinsACTT , CM000669.2:g.107920019_107920022delinsACTT GRCh38
NC_000007.13:g.107560464_107560467delinsACTT , CM000669.1:g.107560464_107560467delinsACTT GRCh37
NC_000007.12:g.107347700_107347703delinsACTT NCBI36
NG_008045.1:g.33879_33882delinsACTT

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*760_*763delinsACTT MANE Select ENSP00000205402.3:n.*760_*763delinsACTT
ENST00000205402.9:c.*760_*763delinsACTT ENSP00000205402.3:n.*760_*763delinsACTT
ENST00000417551.5:c.*124+636_*124+639delinsACTT ENSP00000390667.1:n.*124+636_*124+639delinsACTT
NM_000108.4:c.*760_*763delinsACTT NP_000099.2:n.*760_*763delinsACTT
NM_001289750.1:c.*760_*763delinsACTT NP_001276679.1:n.*760_*763delinsACTT
NM_001289751.1:c.*760_*763delinsACTT NP_001276680.1:n.*760_*763delinsACTT
NM_001289752.1:c.*760_*763delinsACTT NP_001276681.1:n.*760_*763delinsACTT
NM_000108.5:c.*760_*763delinsACTT MANE Select NP_000099.2:n.*760_*763delinsACTT
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