Canonical Allele Identifier: CA2684458235
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107916902_107916903insG , CM000669.2:g.107916902_107916903insG GRCh38
NC_000007.13:g.107557347_107557348insG , CM000669.1:g.107557347_107557348insG GRCh37
NC_000007.12:g.107344583_107344584insG NCBI36
NG_008045.1:g.30762_30763insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.984_985insG MANE Select ENSP00000205402.3:p.Ile329AspfsTer2
ENST00000205402.9:c.984_985insG ENSP00000205402.3:p.Ile329AspfsTer2
ENST00000415325.5:c.*658_*659insG ENSP00000402593.1:n.*658_*659insG
ENST00000417551.5:c.984_985insG ENSP00000390667.1:p.Ile329AspfsTer2
ENST00000437604.6:c.840_841insG ENSP00000387542.2:p.Ile281AspfsTer2
ENST00000440410.5:c.915_916insG ENSP00000417016.1:p.Ile306AspfsTer2
NM_000108.4:c.984_985insG NP_000099.2:p.Ile329AspfsTer2
NM_001289750.1:c.687_688insG NP_001276679.1:p.Ile230AspfsTer2
NM_001289751.1:c.915_916insG NP_001276680.1:p.Ile306AspfsTer2
NM_001289752.1:c.840_841insG NP_001276681.1:p.Ile281AspfsTer2
NM_000108.5:c.984_985insG MANE Select NP_000099.2:p.Ile329AspfsTer2