Canonical Allele Identifier: CA344076109

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203811G>C , CM000663.2:g.193203811G>C	GRCh38
NC_000001.10:g.193172941G>C , CM000663.1:g.193172941G>C	GRCh37
NC_000001.9:g.191439564G>C	NCBI36
NG_012691.1:g.86854G>C , LRG_507:g.86854G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.989G>C MANE Select	ENSP00000356405.4:p.Arg330Pro
ENST00000635846.1:c.746G>C	ENSP00000490035.1:p.Arg249Pro
ENST00000643006.1:c.1057G>C	ENSP00000496633.1:p.Gly353Arg
ENST00000648071.1:c.*965G>C	ENSP00000497513.1:n.*965G>C
ENST00000649613.1:n.239G>C
ENST00000649895.1:n.1207G>C
ENST00000650197.1:c.989G>C	ENSP00000496929.1:p.Arg330Pro
ENST00000367435.3:c.989G>C	ENSP00000356405.3:p.Arg330Pro
NM_024529.4:c.989G>C , LRG_507t1:c.989G>C	NP_078805.3:p.Arg330Pro
NM_024529.5:c.989G>C MANE Select	NP_078805.3:p.Arg330Pro