Canonical Allele Identifier: CA457109397
Gene: DLD HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107557757G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917312G>A , CM000669.2:g.107917312G>A GRCh38
NC_000007.13:g.107557757G>A , CM000669.1:g.107557757G>A GRCh37
NC_000007.12:g.107344993G>A NCBI36
NG_008045.1:g.31172G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.1086G>A MANE Select ENSP00000205402.3:p.Leu362=
ENST00000205402.9:c.1086G>A ENSP00000205402.3:p.Leu362=
ENST00000415325.5:c.*760G>A ENSP00000402593.1:n.*760G>A
ENST00000417551.5:c.1086G>A ENSP00000390667.1:p.Leu362=
ENST00000437604.6:c.942G>A ENSP00000387542.2:p.Leu314=
ENST00000440410.5:c.1017G>A ENSP00000417016.1:p.Leu339=
NM_000108.4:c.1086G>A NP_000099.2:p.Leu362=
NM_001289750.1:c.789G>A NP_001276679.1:p.Leu263=
NM_001289751.1:c.1017G>A NP_001276680.1:p.Leu339=
NM_001289752.1:c.942G>A NP_001276681.1:p.Leu314=
NM_000108.5:c.1086G>A MANE Select NP_000099.2:p.Leu362=