Canonical Allele Identifier: CA1732859949

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917076_107917077delinsGT , CM000669.2:g.107917076_107917077delinsGT	GRCh38
NC_000007.13:g.107557521_107557522delinsGT , CM000669.1:g.107557521_107557522delinsGT	GRCh37
NC_000007.12:g.107344757_107344758delinsGT	NCBI36
NG_008045.1:g.30936_30937delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1046+112_1046+113delinsGT MANE Select	ENSP00000205402.3:n.1046+112_1046+113delinsGT
ENST00000205402.9:c.1046+112_1046+113delinsGT	ENSP00000205402.3:n.1046+112_1046+113delinsGT
ENST00000415325.5:c.*720+112_*720+113delinsGT	ENSP00000402593.1:n.*720+112_*720+113delinsGT
ENST00000417551.5:c.1046+112_1046+113delinsGT	ENSP00000390667.1:n.1046+112_1046+113delinsGT
ENST00000437604.6:c.902+112_902+113delinsGT	ENSP00000387542.2:n.902+112_902+113delinsGT
ENST00000440410.5:c.977+112_977+113delinsGT	ENSP00000417016.1:n.977+112_977+113delinsGT
NM_000108.4:c.1046+112_1046+113delinsGT	NP_000099.2:n.1046+112_1046+113delinsGT
NM_001289750.1:c.749+112_749+113delinsGT	NP_001276679.1:n.749+112_749+113delinsGT
NM_001289751.1:c.977+112_977+113delinsGT	NP_001276680.1:n.977+112_977+113delinsGT
NM_001289752.1:c.902+112_902+113delinsGT	NP_001276681.1:n.902+112_902+113delinsGT
NM_000108.5:c.1046+112_1046+113delinsGT MANE Select	NP_000099.2:n.1046+112_1046+113delinsGT