Canonical Allele Identifier: CA831207864

Gene: DLD

Linked Data

• dbSNP Id: rs1314120153
• gnomAD v4: 7-107915431-AATT-A
• MyVariant Identifiers: chr7:g.107555877_107555879del (hg19) ; chr7:g.107915432_107915434del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915436_107915438del , CM000669.2:g.107915436_107915438del	GRCh38
NC_000007.13:g.107555881_107555883del , CM000669.1:g.107555881_107555883del	GRCh37
NC_000007.12:g.107343117_107343119del	NCBI36
NG_008045.1:g.29296_29298del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.685-70_685-68del MANE Select	ENSP00000205402.3:n.685-70_685-68del
ENST00000205402.9:c.685-70_685-68del	ENSP00000205402.3:n.685-70_685-68del
ENST00000415325.5:c.*359-70_*359-68del	ENSP00000402593.1:n.*359-70_*359-68del
ENST00000417551.5:c.685-70_685-68del	ENSP00000390667.1:n.685-70_685-68del
ENST00000437604.6:c.541-70_541-68del	ENSP00000387542.2:n.541-70_541-68del
ENST00000440410.5:c.616-70_616-68del	ENSP00000417016.1:n.616-70_616-68del
ENST00000451081.5:c.*428-70_*428-68del	ENSP00000388077.1:n.*428-70_*428-68del
NM_000108.4:c.685-70_685-68del	NP_000099.2:n.685-70_685-68del
NM_001289750.1:c.388-70_388-68del	NP_001276679.1:n.388-70_388-68del
NM_001289751.1:c.616-70_616-68del	NP_001276680.1:n.616-70_616-68del
NM_001289752.1:c.541-70_541-68del	NP_001276681.1:n.541-70_541-68del
NM_000108.5:c.685-70_685-68del MANE Select	NP_000099.2:n.685-70_685-68del