Canonical Allele Identifier: CA2684458500

Gene: DLD

Linked Data

• gnomAD v4: 7-107917058-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917060del , CM000669.2:g.107917060del	GRCh38
NC_000007.13:g.107557505del , CM000669.1:g.107557505del	GRCh37
NC_000007.12:g.107344741del	NCBI36
NG_008045.1:g.30920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1046+96del MANE Select	ENSP00000205402.3:n.1046+96del
ENST00000205402.9:c.1046+96del	ENSP00000205402.3:n.1046+96del
ENST00000415325.5:c.*720+96del	ENSP00000402593.1:n.*720+96del
ENST00000417551.5:c.1046+96del	ENSP00000390667.1:n.1046+96del
ENST00000437604.6:c.902+96del	ENSP00000387542.2:n.902+96del
ENST00000440410.5:c.977+96del	ENSP00000417016.1:n.977+96del
NM_000108.4:c.1046+96del	NP_000099.2:n.1046+96del
NM_001289750.1:c.749+96del	NP_001276679.1:n.749+96del
NM_001289751.1:c.977+96del	NP_001276680.1:n.977+96del
NM_001289752.1:c.902+96del	NP_001276681.1:n.902+96del
NM_000108.5:c.1046+96del MANE Select	NP_000099.2:n.1046+96del