Canonical Allele Identifier: CA457109837

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107559590_107559591insCTGACC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919147_107919152dup , CM000669.2:g.107919147_107919152dup	GRCh38
NC_000007.13:g.107559592_107559597dup , CM000669.1:g.107559592_107559597dup	GRCh37
NC_000007.12:g.107346828_107346833dup	NCBI36
NG_008045.1:g.33007_33012dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1465-47_1465-42dup MANE Select	ENSP00000205402.3:n.1465-47_1465-42dup
ENST00000205402.9:c.1465-47_1465-42dup	ENSP00000205402.3:n.1465-47_1465-42dup
ENST00000415325.5:c.*1139-47_*1139-42dup	ENSP00000402593.1:n.*1139-47_*1139-42dup
ENST00000417551.5:c.1465-47_1465-42dup	ENSP00000390667.1:n.1465-47_1465-42dup
ENST00000437604.6:c.1321-47_1321-42dup	ENSP00000387542.2:n.1321-47_1321-42dup
ENST00000440410.5:c.1396-47_1396-42dup	ENSP00000417016.1:n.1396-47_1396-42dup
NM_000108.4:c.1465-47_1465-42dup	NP_000099.2:n.1465-47_1465-42dup
NM_001289750.1:c.1168-47_1168-42dup	NP_001276679.1:n.1168-47_1168-42dup
NM_001289751.1:c.1396-47_1396-42dup	NP_001276680.1:n.1396-47_1396-42dup
NM_001289752.1:c.1321-47_1321-42dup	NP_001276681.1:n.1321-47_1321-42dup
NM_000108.5:c.1465-47_1465-42dup MANE Select	NP_000099.2:n.1465-47_1465-42dup