Canonical Allele Identifier: CA2747148456

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251964T>C , CM000663.2:g.193251964T>C	GRCh38
NC_000001.10:g.193221094T>C , CM000663.1:g.193221094T>C	GRCh37
NC_000001.9:g.191487717T>C	NCBI36
NG_012691.1:g.135007T>C , LRG_507:g.135007T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*1252T>C MANE Select	ENSP00000356405.4:n.*1252T>C
ENST00000635846.1:c.*1252T>C	ENSP00000490035.1:n.*1252T>C
ENST00000643006.1:c.*1758T>C	ENSP00000496633.1:n.*1758T>C
ENST00000367435.3:c.*1252T>C	ENSP00000356405.3:n.*1252T>C
NM_024529.4:c.*1252T>C , LRG_507t1:c.*1252T>C	NP_078805.3:n.*1252T>C
NM_024529.5:c.*1252T>C MANE Select	NP_078805.3:n.*1252T>C