Canonical Allele Identifier: CA913111804

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107559523_107559525del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919078_107919080del , CM000669.2:g.107919078_107919080del	GRCh38
NC_000007.13:g.107559523_107559525del , CM000669.1:g.107559523_107559525del	GRCh37
NC_000007.12:g.107346759_107346761del	NCBI36
NG_008045.1:g.32938_32940del

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1443_1445del MANE Select	ENSP00000205402.3:p.Arg482del
ENST00000205402.9:c.1443_1445del	ENSP00000205402.3:p.Arg482del
ENST00000415325.5:c.*1117_*1119del	ENSP00000402593.1:n.*1117_*1119del
ENST00000417551.5:c.1443_1445del	ENSP00000390667.1:p.Arg482del
ENST00000437604.6:c.1299_1301del	ENSP00000387542.2:p.Arg434del
ENST00000440410.5:c.1374_1376del	ENSP00000417016.1:p.Arg459del
NM_000108.4:c.1443_1445del	NP_000099.2:p.Arg482del
NM_001289750.1:c.1146_1148del	NP_001276679.1:p.Arg383del
NM_001289751.1:c.1374_1376del	NP_001276680.1:p.Arg459del
NM_001289752.1:c.1299_1301del	NP_001276681.1:p.Arg434del
NM_000108.5:c.1443_1445del MANE Select	NP_000099.2:p.Arg482del