Canonical Allele Identifier: CA577039463
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs1199296743
gnomAD v2: 7-107560802-A-T
gnomAD v3: 7-107920357-A-T
gnomAD v4: 7-107920357-A-T
MyVariant Identifiers: chr7:g.107560802A>T (hg19) chr7:g.107920357A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920357A>T , CM000669.2:g.107920357A>T GRCh38
NC_000007.13:g.107560802A>T , CM000669.1:g.107560802A>T GRCh37
NC_000007.12:g.107348038A>T NCBI36
NG_008045.1:g.34217A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*1098A>T MANE Select ENSP00000205402.3:n.*1098A>T
ENST00000205402.9:c.*1098A>T ENSP00000205402.3:n.*1098A>T
ENST00000417551.5:c.*124+974A>T ENSP00000390667.1:n.*124+974A>T
NM_000108.4:c.*1098A>T NP_000099.2:n.*1098A>T
NM_001289750.1:c.*1098A>T NP_001276679.1:n.*1098A>T
NM_001289751.1:c.*1098A>T NP_001276680.1:n.*1098A>T
NM_001289752.1:c.*1098A>T NP_001276681.1:n.*1098A>T
NM_000108.5:c.*1098A>T MANE Select NP_000099.2:n.*1098A>T
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