Canonical Allele Identifier: CA831211714

Gene: DLD

Linked Data

• dbSNP Id: rs1195907430
• gnomAD v3: 7-107920358-A-G
• gnomAD v4: 7-107920358-A-G
• MyVariant Identifiers: chr7:g.107560803A>G (hg19) ; chr7:g.107920358A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107920358A>G , CM000669.2:g.107920358A>G	GRCh38
NC_000007.13:g.107560803A>G , CM000669.1:g.107560803A>G	GRCh37
NC_000007.12:g.107348039A>G	NCBI36
NG_008045.1:g.34218A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.*1099A>G MANE Select	ENSP00000205402.3:n.*1099A>G
ENST00000205402.9:c.*1099A>G	ENSP00000205402.3:n.*1099A>G
ENST00000417551.5:c.*124+975A>G	ENSP00000390667.1:n.*124+975A>G
NM_000108.4:c.*1099A>G	NP_000099.2:n.*1099A>G
NM_001289750.1:c.*1099A>G	NP_001276679.1:n.*1099A>G
NM_001289751.1:c.*1099A>G	NP_001276680.1:n.*1099A>G
NM_001289752.1:c.*1099A>G	NP_001276681.1:n.*1099A>G
NM_000108.5:c.*1099A>G MANE Select	NP_000099.2:n.*1099A>G