Canonical Allele Identifier: CA164259110

Gene: DLD

Linked Data

• dbSNP Id: rs924202258
• gnomAD v2: 7-107559707-TAGA-T
• gnomAD v4: 7-107919262-TAGA-T
• MyVariant Identifiers: chr7:g.107559708_107559710del (hg19) ; chr7:g.107919263_107919265del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919266_107919268del , CM000669.2:g.107919266_107919268del	GRCh38
NC_000007.13:g.107559711_107559713del , CM000669.1:g.107559711_107559713del	GRCh37
NC_000007.12:g.107346947_107346949del	NCBI36
NG_008045.1:g.33126_33128del

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.*7_*9del MANE Select	ENSP00000205402.3:n.*7_*9del
ENST00000205402.9:c.*7_*9del	ENSP00000205402.3:n.*7_*9del
ENST00000415325.5:c.*1211_*1213del	ENSP00000402593.1:n.*1211_*1213del
ENST00000417551.5:c.*7_*9del	ENSP00000390667.1:n.*7_*9del
ENST00000437604.6:c.*7_*9del	ENSP00000387542.2:n.*7_*9del
ENST00000440410.5:c.*7_*9del	ENSP00000417016.1:n.*7_*9del
NM_000108.4:c.*7_*9del	NP_000099.2:n.*7_*9del
NM_001289750.1:c.*7_*9del	NP_001276679.1:n.*7_*9del
NM_001289751.1:c.*7_*9del	NP_001276680.1:n.*7_*9del
NM_001289752.1:c.*7_*9del	NP_001276681.1:n.*7_*9del
NM_000108.5:c.*7_*9del MANE Select	NP_000099.2:n.*7_*9del