Canonical Allele Identifier: CA1732859900
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107916934T= , CM000669.2:g.107916934T= GRCh38
NC_000007.13:g.107557379T= , CM000669.1:g.107557379T= GRCh37
NC_000007.12:g.107344615T= NCBI36
NG_008045.1:g.30794T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1016T= MANE Select ENSP00000205402.3:p.Val339=
ENST00000205402.9:c.1016T= ENSP00000205402.3:p.Val339=
ENST00000415325.5:c.*690T= ENSP00000402593.1:n.*690T=
ENST00000417551.5:c.1016T= ENSP00000390667.1:p.Val339=
ENST00000437604.6:c.872T= ENSP00000387542.2:p.Val291=
ENST00000440410.5:c.947T= ENSP00000417016.1:p.Val316=
NM_000108.4:c.1016T= NP_000099.2:p.Val339=
NM_001289750.1:c.719T= NP_001276679.1:p.Val240=
NM_001289751.1:c.947T= NP_001276680.1:p.Val316=
NM_001289752.1:c.872T= NP_001276681.1:p.Val291=
NM_000108.5:c.1016T= MANE Select NP_000099.2:p.Val339=