Canonical Allele Identifier: CA1216113440

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122288T= , CM000663.2:g.193122288T=	GRCh38
NC_000001.10:g.193091418T= , CM000663.1:g.193091418T=	GRCh37
NC_000001.9:g.191358041T=	NCBI36
NG_012691.1:g.5331T= , LRG_507:g.5331T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.88T= MANE Select	ENSP00000356405.4:p.Phe30=
ENST00000635846.1:c.88T=	ENSP00000490035.1:p.Phe30=
ENST00000643006.1:c.88T=	ENSP00000496633.1:p.Phe30=
ENST00000643784.1:c.88T=	ENSP00000494944.1:p.Phe30=
ENST00000648071.1:c.88T=	ENSP00000497513.1:p.Phe30=
ENST00000649606.1:n.101T=
ENST00000649895.1:n.306T=
ENST00000650197.1:c.88T=	ENSP00000496929.1:p.Phe30=
ENST00000367435.3:c.88T=	ENSP00000356405.3:p.Phe30=
NM_024529.4:c.88T= , LRG_507t1:c.88T=	NP_078805.3:p.Phe30=
XM_006711537.2:c.88T=	XP_006711600.1:p.Phe30=
XM_006711537.4:c.88T=	XP_006711600.1:p.Phe30=
XR_001738350.1:n.1369A=
NM_024529.5:c.88T= MANE Select	NP_078805.3:p.Phe30=