Canonical Allele Identifier: CA1216149982

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203829C= , CM000663.2:g.193203829C=	GRCh38
NC_000001.10:g.193172959C= , CM000663.1:g.193172959C=	GRCh37
NC_000001.9:g.191439582C=	NCBI36
NG_012691.1:g.86872C= , LRG_507:g.86872C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1007C= MANE Select	ENSP00000356405.4:p.Ala336=
ENST00000635846.1:c.764C=	ENSP00000490035.1:p.Ala255=
ENST00000643006.1:c.1075C=	ENSP00000496633.1:p.Gln359=
ENST00000648071.1:c.*983C=	ENSP00000497513.1:n.*983C=
ENST00000649613.1:n.257C=
ENST00000649895.1:n.1225C=
ENST00000650197.1:c.1007C=	ENSP00000496929.1:p.Ala336=
ENST00000367435.3:c.1007C=	ENSP00000356405.3:p.Ala336=
NM_024529.4:c.1007C= , LRG_507t1:c.1007C=	NP_078805.3:p.Ala336=
NM_024529.5:c.1007C= MANE Select	NP_078805.3:p.Ala336=