Canonical Allele Identifier: CA831211592
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs1411262026
gnomAD v3: 7-107920112-TC-T
gnomAD v4: 7-107920112-TC-T
MyVariant Identifiers: chr7:g.107560558del (hg19) chr7:g.107920113del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920114del , CM000669.2:g.107920114del GRCh38
NC_000007.13:g.107560559del , CM000669.1:g.107560559del GRCh37
NC_000007.12:g.107347795del NCBI36
NG_008045.1:g.33974del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*855del MANE Select ENSP00000205402.3:n.*855del
ENST00000205402.9:c.*855del ENSP00000205402.3:n.*855del
ENST00000417551.5:c.*124+731del ENSP00000390667.1:n.*124+731del
NM_000108.4:c.*855del NP_000099.2:n.*855del
NM_001289750.1:c.*855del NP_001276679.1:n.*855del
NM_001289751.1:c.*855del NP_001276680.1:n.*855del
NM_001289752.1:c.*855del NP_001276681.1:n.*855del
NM_000108.5:c.*855del MANE Select NP_000099.2:n.*855del
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