Canonical Allele Identifier: CA164259312
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs948689084
gnomAD v2: 7-107560449-G-GT
gnomAD v3: 7-107920004-G-GT
gnomAD v4: 7-107920004-G-GT
MyVariant Identifiers: chr7:g.107560449_107560450insT (hg19) chr7:g.107920004_107920005insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920012dup , CM000669.2:g.107920012dup GRCh38
NC_000007.13:g.107560457dup , CM000669.1:g.107560457dup GRCh37
NC_000007.12:g.107347693dup NCBI36
NG_008045.1:g.33872dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*753dup MANE Select ENSP00000205402.3:n.*753dup
ENST00000205402.9:c.*753dup ENSP00000205402.3:n.*753dup
ENST00000417551.5:c.*124+629dup ENSP00000390667.1:n.*124+629dup
NM_000108.4:c.*753dup NP_000099.2:n.*753dup
NM_001289750.1:c.*753dup NP_001276679.1:n.*753dup
NM_001289751.1:c.*753dup NP_001276680.1:n.*753dup
NM_001289752.1:c.*753dup NP_001276681.1:n.*753dup
NM_000108.5:c.*753dup MANE Select NP_000099.2:n.*753dup
Search 100 bp 5'
Search 100 bp 3'