Canonical Allele Identifier: CA422491612

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203797G>A , CM000663.2:g.193203797G>A	GRCh38
NC_000001.10:g.193172927G>A , CM000663.1:g.193172927G>A	GRCh37
NC_000001.9:g.191439550G>A	NCBI36
NG_012691.1:g.86840G>A , LRG_507:g.86840G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.975G>A MANE Select	NP_078805.3:p.Glu325=
ENST00000367435.5:c.975G>A MANE Select	ENSP00000356405.4:p.Glu325=
NM_024529.4:c.975G>A , LRG_507t1:c.975G>A	NP_078805.3:p.Glu325=
ENST00000367435.3:c.975G>A	ENSP00000356405.3:p.Glu325=
ENST00000635846.1:c.732G>A	ENSP00000490035.1:p.Glu244=
ENST00000643006.1:c.1043G>A	ENSP00000496633.1:p.Arg348Lys
ENST00000648071.1:c.*951G>A	ENSP00000497513.1:n.*951G>A
ENST00000649613.1:n.225G>A
ENST00000649895.1:n.1193G>A
ENST00000650197.1:c.975G>A	ENSP00000496929.1:p.Glu325=