Canonical Allele Identifier: CA1216122097

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142024A= , CM000663.2:g.193142024A=	GRCh38
NC_000001.10:g.193111154A= , CM000663.1:g.193111154A=	GRCh37
NC_000001.9:g.191377777A=	NCBI36
NG_012691.1:g.25067A= , LRG_507:g.25067A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.687A= MANE Select	ENSP00000356405.4:p.Arg229=
ENST00000635846.1:c.687A=	ENSP00000490035.1:p.Arg229=
ENST00000643006.1:c.687A=	ENSP00000496633.1:p.Arg229=
ENST00000643784.1:c.*163A=	ENSP00000494944.1:n.*163A=
ENST00000647662.1:n.588A=
ENST00000648071.1:c.*663A=	ENSP00000497513.1:n.*663A=
ENST00000649606.1:n.700A=
ENST00000649895.1:n.905A=
ENST00000650197.1:c.687A=	ENSP00000496929.1:p.Arg229=
ENST00000367435.3:c.687A=	ENSP00000356405.3:p.Arg229=
NM_024529.4:c.687A= , LRG_507t1:c.687A=	NP_078805.3:p.Arg229=
XM_006711537.2:c.687A=	XP_006711600.1:p.Arg229=
XM_006711537.4:c.687A=	XP_006711600.1:p.Arg229=
NM_024529.5:c.687A= MANE Select	NP_078805.3:p.Arg229=