Canonical Allele Identifier: CA1303868

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193249765C>G , CM000663.2:g.193249765C>G	GRCh38
NC_000001.10:g.193218895C>G , CM000663.1:g.193218895C>G	GRCh37
NC_000001.9:g.191485518C>G	NCBI36
NG_012691.1:g.132808C>G , LRG_507:g.132808C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.1453C>G MANE Select	NP_078805.3:p.Leu485Val
ENST00000367435.5:c.1453C>G MANE Select	ENSP00000356405.4:p.Leu485Val
NM_024529.4:c.1453C>G , LRG_507t1:c.1453C>G	NP_078805.3:p.Leu485Val
ENST00000367435.3:c.1453C>G	ENSP00000356405.3:p.Leu485Val
ENST00000477868.1:n.165C>G
ENST00000635846.1:c.1210C>G	ENSP00000490035.1:p.Leu404Val
ENST00000643006.1:c.*363C>G	ENSP00000496633.1:n.*363C>G
ENST00000648071.1:c.*1429C>G	ENSP00000497513.1:n.*1429C>G
ENST00000649613.1:n.703C>G
ENST00000650197.1:c.*151C>G	ENSP00000496929.1:n.*151C>G