Canonical Allele Identifier: CA1732860081

Gene: DLD

Linked Data

• dbSNP Id: rs2032296896

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917446_107917447insAACACAAT , CM000669.2:g.107917446_107917447insAACACAAT	GRCh38
NC_000007.13:g.107557891_107557892insAACACAAT , CM000669.1:g.107557891_107557892insAACACAAT	GRCh37
NC_000007.12:g.107345127_107345128insAACACAAT	NCBI36
NG_008045.1:g.31306_31307insAACACAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1220_1221insAACACAAT MANE Select	ENSP00000205402.3:p.Gln408ThrfsTer5
ENST00000205402.9:c.1220_1221insAACACAAT	ENSP00000205402.3:p.Gln408ThrfsTer5
ENST00000415325.5:c.*894_*895insAACACAAT	ENSP00000402593.1:n.*894_*895insAACACAAT
ENST00000417551.5:c.1220_1221insAACACAAT	ENSP00000390667.1:p.Gln408ThrfsTer5
ENST00000437604.6:c.1076_1077insAACACAAT	ENSP00000387542.2:p.Gln360ThrfsTer5
ENST00000440410.5:c.1151_1152insAACACAAT	ENSP00000417016.1:p.Gln385ThrfsTer5
NM_000108.4:c.1220_1221insAACACAAT	NP_000099.2:p.Gln408ThrfsTer5
NM_001289750.1:c.923_924insAACACAAT	NP_001276679.1:p.Gln309ThrfsTer5
NM_001289751.1:c.1151_1152insAACACAAT	NP_001276680.1:p.Gln385ThrfsTer5
NM_001289752.1:c.1076_1077insAACACAAT	NP_001276681.1:p.Gln360ThrfsTer5
NM_000108.5:c.1220_1221insAACACAAT MANE Select	NP_000099.2:p.Gln408ThrfsTer5