Canonical Allele Identifier: CA1732860786

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919165_107919166delinsAT , CM000669.2:g.107919165_107919166delinsAT	GRCh38
NC_000007.13:g.107559610_107559611delinsAT , CM000669.1:g.107559610_107559611delinsAT	GRCh37
NC_000007.12:g.107346846_107346847delinsAT	NCBI36
NG_008045.1:g.33025_33026delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1465-29_1465-28delinsAT MANE Select	ENSP00000205402.3:n.1465-29_1465-28delinsAT
ENST00000205402.9:c.1465-29_1465-28delinsAT	ENSP00000205402.3:n.1465-29_1465-28delinsAT
ENST00000415325.5:c.*1139-29_*1139-28delinsAT	ENSP00000402593.1:n.*1139-29_*1139-28delinsAT
ENST00000417551.5:c.1465-29_1465-28delinsAT	ENSP00000390667.1:n.1465-29_1465-28delinsAT
ENST00000437604.6:c.1321-29_1321-28delinsAT	ENSP00000387542.2:n.1321-29_1321-28delinsAT
ENST00000440410.5:c.1396-29_1396-28delinsAT	ENSP00000417016.1:n.1396-29_1396-28delinsAT
NM_000108.4:c.1465-29_1465-28delinsAT	NP_000099.2:n.1465-29_1465-28delinsAT
NM_001289750.1:c.1168-29_1168-28delinsAT	NP_001276679.1:n.1168-29_1168-28delinsAT
NM_001289751.1:c.1396-29_1396-28delinsAT	NP_001276680.1:n.1396-29_1396-28delinsAT
NM_001289752.1:c.1321-29_1321-28delinsAT	NP_001276681.1:n.1321-29_1321-28delinsAT
NM_000108.5:c.1465-29_1465-28delinsAT MANE Select	NP_000099.2:n.1465-29_1465-28delinsAT