Canonical Allele Identifier: CA2649631026
Gene: CDC73 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251492C>A , CM000663.2:g.193251492C>A GRCh38
NC_000001.10:g.193220622C>A , CM000663.1:g.193220622C>A GRCh37
NC_000001.9:g.191487245C>A NCBI36
NG_012691.1:g.134535C>A , LRG_507:g.134535C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*780C>A MANE Select ENSP00000356405.4:n.*780C>A
ENST00000635846.1:c.*780C>A ENSP00000490035.1:n.*780C>A
ENST00000643006.1:c.*1286C>A ENSP00000496633.1:n.*1286C>A
ENST00000367435.3:c.*780C>A ENSP00000356405.3:n.*780C>A
NM_024529.4:c.*780C>A , LRG_507t1:c.*780C>A NP_078805.3:n.*780C>A
NM_024529.5:c.*780C>A MANE Select NP_078805.3:n.*780C>A