Canonical Allele Identifier: CA1216122089

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142001C= , CM000663.2:g.193142001C=	GRCh38
NC_000001.10:g.193111131C= , CM000663.1:g.193111131C=	GRCh37
NC_000001.9:g.191377754C=	NCBI36
NG_012691.1:g.25044C= , LRG_507:g.25044C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.664C= MANE Select	ENSP00000356405.4:p.Arg222=
ENST00000635846.1:c.664C=	ENSP00000490035.1:p.Arg222=
ENST00000643006.1:c.664C=	ENSP00000496633.1:p.Arg222=
ENST00000643784.1:c.*140C=	ENSP00000494944.1:n.*140C=
ENST00000647662.1:n.565C=
ENST00000648071.1:c.*640C=	ENSP00000497513.1:n.*640C=
ENST00000649606.1:n.677C=
ENST00000649895.1:n.882C=
ENST00000650197.1:c.664C=	ENSP00000496929.1:p.Arg222=
ENST00000367435.3:c.664C=	ENSP00000356405.3:p.Arg222=
NM_024529.4:c.664C= , LRG_507t1:c.664C=	NP_078805.3:p.Arg222=
XM_006711537.2:c.664C=	XP_006711600.1:p.Arg222=
XM_006711537.4:c.664C=	XP_006711600.1:p.Arg222=
NM_024529.5:c.664C= MANE Select	NP_078805.3:p.Arg222=