Canonical Allele Identifier: CA913111801
Gene: DLD HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107556126dup (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915681dup , CM000669.2:g.107915681dup GRCh38
NC_000007.13:g.107556126dup , CM000669.1:g.107556126dup GRCh37
NC_000007.12:g.107343362dup NCBI36
NG_008045.1:g.29541dup

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.860dup MANE Select ENSP00000205402.3:p.Ile289AsnfsTer2
ENST00000205402.9:c.860dup ENSP00000205402.3:p.Ile289AsnfsTer2
ENST00000415325.5:c.*534dup ENSP00000402593.1:n.*534dup
ENST00000417551.5:c.860dup ENSP00000390667.1:p.Ile289AsnfsTer2
ENST00000437604.6:c.716dup ENSP00000387542.2:p.Ile241AsnfsTer2
ENST00000440410.5:c.791dup ENSP00000417016.1:p.Ile266AsnfsTer2
NM_000108.4:c.860dup NP_000099.2:p.Ile289AsnfsTer2
NM_001289750.1:c.563dup NP_001276679.1:p.Ile190AsnfsTer2
NM_001289751.1:c.791dup NP_001276680.1:p.Ile266AsnfsTer2
NM_001289752.1:c.716dup NP_001276681.1:p.Ile241AsnfsTer2
NM_000108.5:c.860dup MANE Select NP_000099.2:p.Ile289AsnfsTer2