Canonical Allele Identifier: CA577039476
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs1193912163
gnomAD v2: 7-107561177-C-T
gnomAD v3: 7-107920732-C-T
gnomAD v4: 7-107920732-C-T
MyVariant Identifiers: chr7:g.107561177C>T (hg19) chr7:g.107920732C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920732C>T , CM000669.2:g.107920732C>T GRCh38
NC_000007.13:g.107561177C>T , CM000669.1:g.107561177C>T GRCh37
NC_000007.12:g.107348413C>T NCBI36
NG_008045.1:g.34592C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*1473C>T MANE Select ENSP00000205402.3:n.*1473C>T
ENST00000205402.9:c.*1473C>T ENSP00000205402.3:n.*1473C>T
ENST00000417551.5:c.*124+1349C>T ENSP00000390667.1:n.*124+1349C>T
NM_000108.4:c.*1473C>T NP_000099.2:n.*1473C>T
NM_001289750.1:c.*1473C>T NP_001276679.1:n.*1473C>T
NM_001289751.1:c.*1473C>T NP_001276680.1:n.*1473C>T
NM_001289752.1:c.*1473C>T NP_001276681.1:n.*1473C>T
NM_000108.5:c.*1473C>T MANE Select NP_000099.2:n.*1473C>T
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