Canonical Allele Identifier: CA2684464633

Gene: DLD

Linked Data

• gnomAD v4: 7-107915439-AGAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915443_107915445del , CM000669.2:g.107915443_107915445del	GRCh38
NC_000007.13:g.107555888_107555890del , CM000669.1:g.107555888_107555890del	GRCh37
NC_000007.12:g.107343124_107343126del	NCBI36
NG_008045.1:g.29303_29305del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.685-63_685-61del MANE Select	ENSP00000205402.3:n.685-63_685-61del
ENST00000205402.9:c.685-63_685-61del	ENSP00000205402.3:n.685-63_685-61del
ENST00000415325.5:c.*359-63_*359-61del	ENSP00000402593.1:n.*359-63_*359-61del
ENST00000417551.5:c.685-63_685-61del	ENSP00000390667.1:n.685-63_685-61del
ENST00000437604.6:c.541-63_541-61del	ENSP00000387542.2:n.541-63_541-61del
ENST00000440410.5:c.616-63_616-61del	ENSP00000417016.1:n.616-63_616-61del
ENST00000451081.5:c.*428-63_*428-61del	ENSP00000388077.1:n.*428-63_*428-61del
NM_000108.4:c.685-63_685-61del	NP_000099.2:n.685-63_685-61del
NM_001289750.1:c.388-63_388-61del	NP_001276679.1:n.388-63_388-61del
NM_001289751.1:c.616-63_616-61del	NP_001276680.1:n.616-63_616-61del
NM_001289752.1:c.541-63_541-61del	NP_001276681.1:n.541-63_541-61del
NM_000108.5:c.685-63_685-61del MANE Select	NP_000099.2:n.685-63_685-61del