Canonical Allele Identifier: CA1216171220

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251909_193251910delinsAT , CM000663.2:g.193251909_193251910delinsAT	GRCh38
NC_000001.10:g.193221039_193221040delinsAT , CM000663.1:g.193221039_193221040delinsAT	GRCh37
NC_000001.9:g.191487662_191487663delinsAT	NCBI36
NG_012691.1:g.134952_134953delinsAT , LRG_507:g.134952_134953delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*1197_*1198delinsAT MANE Select	ENSP00000356405.4:n.*1197_*1198delinsAT
ENST00000635846.1:c.*1197_*1198delinsAT	ENSP00000490035.1:n.*1197_*1198delinsAT
ENST00000643006.1:c.*1703_*1704delinsAT	ENSP00000496633.1:n.*1703_*1704delinsAT
ENST00000367435.3:c.*1197_*1198delinsAT	ENSP00000356405.3:n.*1197_*1198delinsAT
NM_024529.4:c.*1197_*1198delinsAT , LRG_507t1:c.*1197_*1198delinsAT	NP_078805.3:n.*1197_*1198delinsAT
NM_024529.5:c.*1197_*1198delinsAT MANE Select	NP_078805.3:n.*1197_*1198delinsAT