Canonical Allele Identifier: CA1216171248

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251983_193251984delinsAT , CM000663.2:g.193251983_193251984delinsAT	GRCh38
NC_000001.10:g.193221113_193221114delinsAT , CM000663.1:g.193221113_193221114delinsAT	GRCh37
NC_000001.9:g.191487736_191487737delinsAT	NCBI36
NG_012691.1:g.135026_135027delinsAT , LRG_507:g.135026_135027delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*1271_*1272delinsAT MANE Select	ENSP00000356405.4:n.*1271_*1272delinsAT
ENST00000635846.1:c.*1271_*1272delinsAT	ENSP00000490035.1:n.*1271_*1272delinsAT
ENST00000643006.1:c.*1777_*1778delinsAT	ENSP00000496633.1:n.*1777_*1778delinsAT
ENST00000367435.3:c.*1271_*1272delinsAT	ENSP00000356405.3:n.*1271_*1272delinsAT
NM_024529.4:c.*1271_*1272delinsAT , LRG_507t1:c.*1271_*1272delinsAT	NP_078805.3:n.*1271_*1272delinsAT
NM_024529.5:c.*1271_*1272delinsAT MANE Select	NP_078805.3:n.*1271_*1272delinsAT