Canonical Allele Identifier: CA2747148457
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193252003_193252019dup , CM000663.2:g.193252003_193252019dup GRCh38
NC_000001.10:g.193221133_193221149dup , CM000663.1:g.193221133_193221149dup GRCh37
NC_000001.9:g.191487756_191487772dup NCBI36
NG_012691.1:g.135046_135062dup , LRG_507:g.135046_135062dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1291_*1307dup MANE Select ENSP00000356405.4:n.*1291_*1307dup
ENST00000635846.1:c.*1291_*1307dup ENSP00000490035.1:n.*1291_*1307dup
ENST00000643006.1:c.*1797_*1813dup ENSP00000496633.1:n.*1797_*1813dup
ENST00000367435.3:c.*1291_*1307dup ENSP00000356405.3:n.*1291_*1307dup
NM_024529.4:c.*1291_*1307dup , LRG_507t1:c.*1291_*1307dup NP_078805.3:n.*1291_*1307dup
NM_024529.5:c.*1291_*1307dup MANE Select NP_078805.3:n.*1291_*1307dup