Canonical Allele Identifier: CA1732859892
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107916918A= , CM000669.2:g.107916918A= GRCh38
NC_000007.13:g.107557363A= , CM000669.1:g.107557363A= GRCh37
NC_000007.12:g.107344599A= NCBI36
NG_008045.1:g.30778A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1000A= MANE Select ENSP00000205402.3:p.Arg334=
ENST00000205402.9:c.1000A= ENSP00000205402.3:p.Arg334=
ENST00000415325.5:c.*674A= ENSP00000402593.1:n.*674A=
ENST00000417551.5:c.1000A= ENSP00000390667.1:p.Arg334=
ENST00000437604.6:c.856A= ENSP00000387542.2:p.Arg286=
ENST00000440410.5:c.931A= ENSP00000417016.1:p.Arg311=
NM_000108.4:c.1000A= NP_000099.2:p.Arg334=
NM_001289750.1:c.703A= NP_001276679.1:p.Arg235=
NM_001289751.1:c.931A= NP_001276680.1:p.Arg311=
NM_001289752.1:c.856A= NP_001276681.1:p.Arg286=
NM_000108.5:c.1000A= MANE Select NP_000099.2:p.Arg334=