Canonical Allele Identifier: CA157936

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193212472C>A , CM000663.2:g.193212472C>A	GRCh38
NC_000001.10:g.193181602C>A , CM000663.1:g.193181602C>A	GRCh37
NC_000001.9:g.191448225C>A	NCBI36
NG_012691.1:g.95515C>A , LRG_507:g.95515C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1149C>A MANE Select	ENSP00000356405.4:p.Asp383Glu
ENST00000635846.1:c.906C>A	ENSP00000490035.1:p.Asp302Glu
ENST00000643006.1:c.*59C>A	ENSP00000496633.1:n.*59C>A
ENST00000648071.1:c.*1125C>A	ENSP00000497513.1:n.*1125C>A
ENST00000649613.1:n.399C>A
ENST00000649895.1:n.1367C>A
ENST00000650197.1:c.1149C>A	ENSP00000496929.1:p.Asp383Glu
ENST00000367435.3:c.1149C>A	ENSP00000356405.3:p.Asp383Glu
NM_024529.4:c.1149C>A , LRG_507t1:c.1149C>A	NP_078805.3:p.Asp383Glu
NM_024529.5:c.1149C>A MANE Select	NP_078805.3:p.Asp383Glu