Canonical Allele Identifier: CA1732860142

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917588_107917593delinsATATTT , CM000669.2:g.107917588_107917593delinsATATTT	GRCh38
NC_000007.13:g.107558033_107558038delinsATATTT , CM000669.1:g.107558033_107558038delinsATATTT	GRCh37
NC_000007.12:g.107345269_107345274delinsATATTT	NCBI36
NG_008045.1:g.31448_31453delinsATATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1236+126_1236+131delinsATATTT MANE Select	ENSP00000205402.3:n.1236+126_1236+131delinsATATTT
ENST00000205402.9:c.1236+126_1236+131delinsATATTT	ENSP00000205402.3:n.1236+126_1236+131delinsATATTT
ENST00000415325.5:c.*910+126_*910+131delinsATATTT	ENSP00000402593.1:n.*910+126_*910+131delinsATATTT
ENST00000417551.5:c.1236+126_1236+131delinsATATTT	ENSP00000390667.1:n.1236+126_1236+131delinsATATTT
ENST00000437604.6:c.1092+126_1092+131delinsATATTT	ENSP00000387542.2:n.1092+126_1092+131delinsATATTT
ENST00000440410.5:c.1167+126_1167+131delinsATATTT	ENSP00000417016.1:n.1167+126_1167+131delinsATATTT
NM_000108.4:c.1236+126_1236+131delinsATATTT	NP_000099.2:n.1236+126_1236+131delinsATATTT
NM_001289750.1:c.939+126_939+131delinsATATTT	NP_001276679.1:n.939+126_939+131delinsATATTT
NM_001289751.1:c.1167+126_1167+131delinsATATTT	NP_001276680.1:n.1167+126_1167+131delinsATATTT
NM_001289752.1:c.1092+126_1092+131delinsATATTT	NP_001276681.1:n.1092+126_1092+131delinsATATTT
NM_000108.5:c.1236+126_1236+131delinsATATTT MANE Select	NP_000099.2:n.1236+126_1236+131delinsATATTT