Canonical Allele Identifier: CA577039398

Gene: DLD

Linked Data

• dbSNP Id: rs1298810433
• gnomAD v2: 7-107559610-AT-A
• gnomAD v4: 7-107919165-AT-A
• MyVariant Identifiers: chr7:g.107559611del (hg19) ; chr7:g.107919166del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919169del , CM000669.2:g.107919169del	GRCh38
NC_000007.13:g.107559614del , CM000669.1:g.107559614del	GRCh37
NC_000007.12:g.107346850del	NCBI36
NG_008045.1:g.33029del

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1465-25del MANE Select	ENSP00000205402.3:n.1465-25del
ENST00000205402.9:c.1465-25del	ENSP00000205402.3:n.1465-25del
ENST00000415325.5:c.*1139-25del	ENSP00000402593.1:n.*1139-25del
ENST00000417551.5:c.1465-25del	ENSP00000390667.1:n.1465-25del
ENST00000437604.6:c.1321-25del	ENSP00000387542.2:n.1321-25del
ENST00000440410.5:c.1396-25del	ENSP00000417016.1:n.1396-25del
NM_000108.4:c.1465-25del	NP_000099.2:n.1465-25del
NM_001289750.1:c.1168-25del	NP_001276679.1:n.1168-25del
NM_001289751.1:c.1396-25del	NP_001276680.1:n.1396-25del
NM_001289752.1:c.1321-25del	NP_001276681.1:n.1321-25del
NM_000108.5:c.1465-25del MANE Select	NP_000099.2:n.1465-25del