Canonical Allele Identifier: CA164262671
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs1045038895
MyVariant Identifiers: chr7:g.107561189T>C (hg19) chr7:g.107920744T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920744T>C , CM000669.2:g.107920744T>C GRCh38
NC_000007.13:g.107561189T>C , CM000669.1:g.107561189T>C GRCh37
NC_000007.12:g.107348425T>C NCBI36
NG_008045.1:g.34604T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*1485T>C MANE Select ENSP00000205402.3:n.*1485T>C
ENST00000205402.9:c.*1485T>C ENSP00000205402.3:n.*1485T>C
ENST00000417551.5:c.*124+1361T>C ENSP00000390667.1:n.*124+1361T>C
NM_000108.4:c.*1485T>C NP_000099.2:n.*1485T>C
NM_001289750.1:c.*1485T>C NP_001276679.1:n.*1485T>C
NM_001289751.1:c.*1485T>C NP_001276680.1:n.*1485T>C
NM_001289752.1:c.*1485T>C NP_001276681.1:n.*1485T>C
NM_000108.5:c.*1485T>C MANE Select NP_000099.2:n.*1485T>C
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