Canonical Allele Identifier: CA1146244558
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251805C= , CM000663.2:g.193251805C= GRCh38
NC_000001.10:g.193220935C= , CM000663.1:g.193220935C= GRCh37
NC_000001.9:g.191487558C= NCBI36
NG_012691.1:g.134848C= , LRG_507:g.134848C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1093C= MANE Select ENSP00000356405.4:n.*1093C=
ENST00000635846.1:c.*1093C= ENSP00000490035.1:n.*1093C=
ENST00000643006.1:c.*1599C= ENSP00000496633.1:n.*1599C=
ENST00000367435.3:c.*1093C= ENSP00000356405.3:n.*1093C=
NM_024529.4:c.*1093C= , LRG_507t1:c.*1093C= NP_078805.3:n.*1093C=
NM_024529.5:c.*1093C= MANE Select NP_078805.3:n.*1093C=