Canonical Allele Identifier: CA1732860829

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919266_107919267delinsAG , CM000669.2:g.107919266_107919267delinsAG	GRCh38
NC_000007.13:g.107559711_107559712delinsAG , CM000669.1:g.107559711_107559712delinsAG	GRCh37
NC_000007.12:g.107346947_107346948delinsAG	NCBI36
NG_008045.1:g.33126_33127delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*7_*8delinsAG MANE Select	ENSP00000205402.3:n.*7_*8delinsAG
ENST00000205402.9:c.*7_*8delinsAG	ENSP00000205402.3:n.*7_*8delinsAG
ENST00000415325.5:c.*1211_*1212delinsAG	ENSP00000402593.1:n.*1211_*1212delinsAG
ENST00000417551.5:c.*7_*8delinsAG	ENSP00000390667.1:n.*7_*8delinsAG
ENST00000437604.6:c.*7_*8delinsAG	ENSP00000387542.2:n.*7_*8delinsAG
ENST00000440410.5:c.*7_*8delinsAG	ENSP00000417016.1:n.*7_*8delinsAG
NM_000108.4:c.*7_*8delinsAG	NP_000099.2:n.*7_*8delinsAG
NM_001289750.1:c.*7_*8delinsAG	NP_001276679.1:n.*7_*8delinsAG
NM_001289751.1:c.*7_*8delinsAG	NP_001276680.1:n.*7_*8delinsAG
NM_001289752.1:c.*7_*8delinsAG	NP_001276681.1:n.*7_*8delinsAG
NM_000108.5:c.*7_*8delinsAG MANE Select	NP_000099.2:n.*7_*8delinsAG