Canonical Allele Identifier: CA646166888
Gene: CDC73 HGNC NCBI

Linked Data

COSMIC: COSN22145049
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193252007dup , CM000663.2:g.193252007dup GRCh38
NC_000001.10:g.193221137dup , CM000663.1:g.193221137dup GRCh37
NC_000001.9:g.191487760dup NCBI36
NG_012691.1:g.135050dup , LRG_507:g.135050dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1295dup MANE Select ENSP00000356405.4:n.*1295dup
ENST00000635846.1:c.*1295dup ENSP00000490035.1:n.*1295dup
ENST00000643006.1:c.*1801dup ENSP00000496633.1:n.*1801dup
ENST00000367435.3:c.*1295dup ENSP00000356405.3:n.*1295dup
NM_024529.4:c.*1295dup , LRG_507t1:c.*1295dup NP_078805.3:n.*1295dup
NM_024529.5:c.*1295dup MANE Select NP_078805.3:n.*1295dup
Search 100 bp 5'
Search 100 bp 3'