Canonical Allele Identifier: CA1216171181

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251843_193251844delinsTG , CM000663.2:g.193251843_193251844delinsTG	GRCh38
NC_000001.10:g.193220973_193220974delinsTG , CM000663.1:g.193220973_193220974delinsTG	GRCh37
NC_000001.9:g.191487596_191487597delinsTG	NCBI36
NG_012691.1:g.134886_134887delinsTG , LRG_507:g.134886_134887delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*1131_*1132delinsTG MANE Select	ENSP00000356405.4:n.*1131_*1132delinsTG
ENST00000635846.1:c.*1131_*1132delinsTG	ENSP00000490035.1:n.*1131_*1132delinsTG
ENST00000643006.1:c.*1637_*1638delinsTG	ENSP00000496633.1:n.*1637_*1638delinsTG
ENST00000367435.3:c.*1131_*1132delinsTG	ENSP00000356405.3:n.*1131_*1132delinsTG
NM_024529.4:c.*1131_*1132delinsTG , LRG_507t1:c.*1131_*1132delinsTG	NP_078805.3:n.*1131_*1132delinsTG
NM_024529.5:c.*1131_*1132delinsTG MANE Select	NP_078805.3:n.*1131_*1132delinsTG