Canonical Allele Identifier: CA1732859341
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915601C= , CM000669.2:g.107915601C= GRCh38
NC_000007.13:g.107556046C= , CM000669.1:g.107556046C= GRCh37
NC_000007.12:g.107343282C= NCBI36
NG_008045.1:g.29461C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.780C= MANE Select ENSP00000205402.3:p.Asn260=
ENST00000205402.9:c.780C= ENSP00000205402.3:p.Asn260=
ENST00000415325.5:c.*454C= ENSP00000402593.1:n.*454C=
ENST00000417551.5:c.780C= ENSP00000390667.1:p.Asn260=
ENST00000437604.6:c.636C= ENSP00000387542.2:p.Asn212=
ENST00000440410.5:c.711C= ENSP00000417016.1:p.Asn237=
NM_000108.4:c.780C= NP_000099.2:p.Asn260=
NM_001289750.1:c.483C= NP_001276679.1:p.Asn161=
NM_001289751.1:c.711C= NP_001276680.1:p.Asn237=
NM_001289752.1:c.636C= NP_001276681.1:p.Asn212=
NM_000108.5:c.780C= MANE Select NP_000099.2:p.Asn260=