Canonical Allele Identifier: CA1303255

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122316A>G , CM000663.2:g.193122316A>G	GRCh38
NC_000001.10:g.193091446A>G , CM000663.1:g.193091446A>G	GRCh37
NC_000001.9:g.191358069A>G	NCBI36
NG_012691.1:g.5359A>G , LRG_507:g.5359A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.116A>G MANE Select	NP_078805.3:p.Asn39Ser
ENST00000367435.5:c.116A>G MANE Select	ENSP00000356405.4:p.Asn39Ser
NM_024529.4:c.116A>G , LRG_507t1:c.116A>G	NP_078805.3:p.Asn39Ser
ENST00000367435.3:c.116A>G	ENSP00000356405.3:p.Asn39Ser
ENST00000635846.1:c.116A>G	ENSP00000490035.1:p.Asn39Ser
ENST00000643006.1:c.116A>G	ENSP00000496633.1:p.Asn39Ser
ENST00000643784.1:c.116A>G	ENSP00000494944.1:p.Asn39Ser
ENST00000647662.1:n.17A>G
ENST00000648071.1:c.116A>G	ENSP00000497513.1:p.Asn39Ser
ENST00000649606.1:n.129A>G
ENST00000649895.1:n.334A>G
ENST00000650197.1:c.116A>G	ENSP00000496929.1:p.Asn39Ser
XM_006711537.2:c.116A>G	XP_006711600.1:p.Asn39Ser
XM_006711537.4:c.116A>G	XP_006711600.1:p.Asn39Ser
XR_001738350.1:n.1341T>C