Canonical Allele Identifier: CA1216120481

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193138117A= , CM000663.2:g.193138117A=	GRCh38
NC_000001.10:g.193107247A= , CM000663.1:g.193107247A=	GRCh37
NC_000001.9:g.191373870A=	NCBI36
NG_012691.1:g.21160A= , LRG_507:g.21160A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367435.5:c.456A= MANE Select	ENSP00000356405.4:p.Arg152=
ENST00000635846.1:c.456A=	ENSP00000490035.1:p.Arg152=
ENST00000643006.1:c.456A=	ENSP00000496633.1:p.Arg152=
ENST00000643784.1:c.456A=	ENSP00000494944.1:p.Arg152=
ENST00000647662.1:n.357A=
ENST00000648071.1:c.*432A=	ENSP00000497513.1:n.*432A=
ENST00000649606.1:n.469A=
ENST00000649706.1:n.397A=
ENST00000649895.1:n.674A=
ENST00000650197.1:c.456A=	ENSP00000496929.1:p.Arg152=
ENST00000367435.3:c.456A=	ENSP00000356405.3:p.Arg152=
ENST00000482484.1:n.708A=
NM_024529.4:c.456A= , LRG_507t1:c.456A=	NP_078805.3:p.Arg152=
XM_006711537.2:c.456A=	XP_006711600.1:p.Arg152=
XM_006711537.4:c.456A=	XP_006711600.1:p.Arg152=
NM_024529.5:c.456A= MANE Select	NP_078805.3:p.Arg152=