Canonical Allele Identifier: CA646166886

Gene: CDC73

Linked Data

• COSMIC: COSN15662388

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251903dup , CM000663.2:g.193251903dup	GRCh38
NC_000001.10:g.193221033dup , CM000663.1:g.193221033dup	GRCh37
NC_000001.9:g.191487656dup	NCBI36
NG_012691.1:g.134946dup , LRG_507:g.134946dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*1191dup MANE Select	ENSP00000356405.4:n.*1191dup
ENST00000635846.1:c.*1191dup	ENSP00000490035.1:n.*1191dup
ENST00000643006.1:c.*1697dup	ENSP00000496633.1:n.*1697dup
ENST00000367435.3:c.*1191dup	ENSP00000356405.3:n.*1191dup
NM_024529.4:c.*1191dup , LRG_507t1:c.*1191dup	NP_078805.3:n.*1191dup
NM_024529.5:c.*1191dup MANE Select	NP_078805.3:n.*1191dup