Canonical Allele Identifier: CA1732860138

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917586_107917587delinsAT , CM000669.2:g.107917586_107917587delinsAT	GRCh38
NC_000007.13:g.107558031_107558032delinsAT , CM000669.1:g.107558031_107558032delinsAT	GRCh37
NC_000007.12:g.107345267_107345268delinsAT	NCBI36
NG_008045.1:g.31446_31447delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1236+124_1236+125delinsAT MANE Select	ENSP00000205402.3:n.1236+124_1236+125delinsAT
ENST00000205402.9:c.1236+124_1236+125delinsAT	ENSP00000205402.3:n.1236+124_1236+125delinsAT
ENST00000415325.5:c.*910+124_*910+125delinsAT	ENSP00000402593.1:n.*910+124_*910+125delinsAT
ENST00000417551.5:c.1236+124_1236+125delinsAT	ENSP00000390667.1:n.1236+124_1236+125delinsAT
ENST00000437604.6:c.1092+124_1092+125delinsAT	ENSP00000387542.2:n.1092+124_1092+125delinsAT
ENST00000440410.5:c.1167+124_1167+125delinsAT	ENSP00000417016.1:n.1167+124_1167+125delinsAT
NM_000108.4:c.1236+124_1236+125delinsAT	NP_000099.2:n.1236+124_1236+125delinsAT
NM_001289750.1:c.939+124_939+125delinsAT	NP_001276679.1:n.939+124_939+125delinsAT
NM_001289751.1:c.1167+124_1167+125delinsAT	NP_001276680.1:n.1167+124_1167+125delinsAT
NM_001289752.1:c.1092+124_1092+125delinsAT	NP_001276681.1:n.1092+124_1092+125delinsAT
NM_000108.5:c.1236+124_1236+125delinsAT MANE Select	NP_000099.2:n.1236+124_1236+125delinsAT