Canonical Allele Identifier: CA831211559
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs1163811982
MyVariant Identifiers: chr7:g.107560446A>G (hg19) chr7:g.107920001A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920001A>G , CM000669.2:g.107920001A>G GRCh38
NC_000007.13:g.107560446A>G , CM000669.1:g.107560446A>G GRCh37
NC_000007.12:g.107347682A>G NCBI36
NG_008045.1:g.33861A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*742A>G MANE Select ENSP00000205402.3:n.*742A>G
ENST00000205402.9:c.*742A>G ENSP00000205402.3:n.*742A>G
ENST00000417551.5:c.*124+618A>G ENSP00000390667.1:n.*124+618A>G
NM_000108.4:c.*742A>G NP_000099.2:n.*742A>G
NM_001289750.1:c.*742A>G NP_001276679.1:n.*742A>G
NM_001289751.1:c.*742A>G NP_001276680.1:n.*742A>G
NM_001289752.1:c.*742A>G NP_001276681.1:n.*742A>G
NM_000108.5:c.*742A>G MANE Select NP_000099.2:n.*742A>G
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