Canonical Allele Identifier: CA577039335

Gene: DLD

Linked Data

• dbSNP Id: rs1229240332
• gnomAD v2: 7-107559406-ATG-A
• gnomAD v3: 7-107918961-ATG-A
• gnomAD v4: 7-107918961-ATG-A
• MyVariant Identifiers: chr7:g.107559407_107559408del (hg19) ; chr7:g.107918962_107918963del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107918963_107918964del , CM000669.2:g.107918963_107918964del	GRCh38
NC_000007.13:g.107559408_107559409del , CM000669.1:g.107559408_107559409del	GRCh37
NC_000007.12:g.107346644_107346645del	NCBI36
NG_008045.1:g.32823_32824del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1375-47_1375-46del MANE Select	ENSP00000205402.3:n.1375-47_1375-46del
ENST00000205402.9:c.1375-47_1375-46del	ENSP00000205402.3:n.1375-47_1375-46del
ENST00000415325.5:c.*1049-47_*1049-46del	ENSP00000402593.1:n.*1049-47_*1049-46del
ENST00000417551.5:c.1375-47_1375-46del	ENSP00000390667.1:n.1375-47_1375-46del
ENST00000437604.6:c.1231-47_1231-46del	ENSP00000387542.2:n.1231-47_1231-46del
ENST00000440410.5:c.1306-47_1306-46del	ENSP00000417016.1:n.1306-47_1306-46del
NM_000108.4:c.1375-47_1375-46del	NP_000099.2:n.1375-47_1375-46del
NM_001289750.1:c.1078-47_1078-46del	NP_001276679.1:n.1078-47_1078-46del
NM_001289751.1:c.1306-47_1306-46del	NP_001276680.1:n.1306-47_1306-46del
NM_001289752.1:c.1231-47_1231-46del	NP_001276681.1:n.1231-47_1231-46del
NM_000108.5:c.1375-47_1375-46del MANE Select	NP_000099.2:n.1375-47_1375-46del