Canonical Allele Identifier: CA457109522

Gene: DLD

Linked Data

• gnomAD v4: 7-107917444-A-G
• MyVariant Identifiers: chr7:g.107557889A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917444A>G , CM000669.2:g.107917444A>G	GRCh38
NC_000007.13:g.107557889A>G , CM000669.1:g.107557889A>G	GRCh37
NC_000007.12:g.107345125A>G	NCBI36
NG_008045.1:g.31304A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1218A>G MANE Select	ENSP00000205402.3:p.Glu406=
ENST00000205402.9:c.1218A>G	ENSP00000205402.3:p.Glu406=
ENST00000415325.5:c.*892A>G	ENSP00000402593.1:n.*892A>G
ENST00000417551.5:c.1218A>G	ENSP00000390667.1:p.Glu406=
ENST00000437604.6:c.1074A>G	ENSP00000387542.2:p.Glu358=
ENST00000440410.5:c.1149A>G	ENSP00000417016.1:p.Glu383=
NM_000108.4:c.1218A>G	NP_000099.2:p.Glu406=
NM_001289750.1:c.921A>G	NP_001276679.1:p.Glu307=
NM_001289751.1:c.1149A>G	NP_001276680.1:p.Glu383=
NM_001289752.1:c.1074A>G	NP_001276681.1:p.Glu358=
NM_000108.5:c.1218A>G MANE Select	NP_000099.2:p.Glu406=