Canonical Allele Identifier: CA1142329712

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203811G= , CM000663.2:g.193203811G=	GRCh38
NC_000001.10:g.193172941G= , CM000663.1:g.193172941G=	GRCh37
NC_000001.9:g.191439564G=	NCBI36
NG_012691.1:g.86854G= , LRG_507:g.86854G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.989G= MANE Select	ENSP00000356405.4:p.Arg330=
ENST00000635846.1:c.746G=	ENSP00000490035.1:p.Arg249=
ENST00000643006.1:c.1057G=	ENSP00000496633.1:p.Gly353=
ENST00000648071.1:c.*965G=	ENSP00000497513.1:n.*965G=
ENST00000649613.1:n.239G=
ENST00000649895.1:n.1207G=
ENST00000650197.1:c.989G=	ENSP00000496929.1:p.Arg330=
ENST00000367435.3:c.989G=	ENSP00000356405.3:p.Arg330=
NM_024529.4:c.989G= , LRG_507t1:c.989G=	NP_078805.3:p.Arg330=
NM_024529.5:c.989G= MANE Select	NP_078805.3:p.Arg330=