Canonical Allele Identifier: CA1216171258

Gene: CDC73

Linked Data

• dbSNP Id: rs1678051294

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251997_193251998insCT , CM000663.2:g.193251997_193251998insCT	GRCh38
NC_000001.10:g.193221127_193221128insCT , CM000663.1:g.193221127_193221128insCT	GRCh37
NC_000001.9:g.191487750_191487751insCT	NCBI36
NG_012691.1:g.135040_135041insCT , LRG_507:g.135040_135041insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*1285_*1286insCT MANE Select	ENSP00000356405.4:n.*1285_*1286insCT
ENST00000635846.1:c.*1285_*1286insCT	ENSP00000490035.1:n.*1285_*1286insCT
ENST00000643006.1:c.*1791_*1792insCT	ENSP00000496633.1:n.*1791_*1792insCT
ENST00000367435.3:c.*1285_*1286insCT	ENSP00000356405.3:n.*1285_*1286insCT
NM_024529.4:c.*1285_*1286insCT , LRG_507t1:c.*1285_*1286insCT	NP_078805.3:n.*1285_*1286insCT
NM_024529.5:c.*1285_*1286insCT MANE Select	NP_078805.3:n.*1285_*1286insCT