Canonical Allele Identifier: CA368857682
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107916880A>T , CM000669.2:g.107916880A>T GRCh38
NC_000007.13:g.107557325A>T , CM000669.1:g.107557325A>T GRCh37
NC_000007.12:g.107344561A>T NCBI36
NG_008045.1:g.30740A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.962A>T MANE Select ENSP00000205402.3:p.Asn321Ile
ENST00000205402.9:c.962A>T ENSP00000205402.3:p.Asn321Ile
ENST00000415325.5:c.*636A>T ENSP00000402593.1:n.*636A>T
ENST00000417551.5:c.962A>T ENSP00000390667.1:p.Asn321Ile
ENST00000437604.6:c.818A>T ENSP00000387542.2:p.Asn273Ile
ENST00000440410.5:c.893A>T ENSP00000417016.1:p.Asn298Ile
NM_000108.4:c.962A>T NP_000099.2:p.Asn321Ile
NM_001289750.1:c.665A>T NP_001276679.1:p.Asn222Ile
NM_001289751.1:c.893A>T NP_001276680.1:p.Asn298Ile
NM_001289752.1:c.818A>T NP_001276681.1:p.Asn273Ile
NM_000108.5:c.962A>T MANE Select NP_000099.2:p.Asn321Ile