Canonical Allele Identifier: CA1216171102

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251655A= , CM000663.2:g.193251655A=	GRCh38
NC_000001.10:g.193220785A= , CM000663.1:g.193220785A=	GRCh37
NC_000001.9:g.191487408A=	NCBI36
NG_012691.1:g.134698A= , LRG_507:g.134698A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*943A= MANE Select	ENSP00000356405.4:n.*943A=
ENST00000635846.1:c.*943A=	ENSP00000490035.1:n.*943A=
ENST00000643006.1:c.*1449A=	ENSP00000496633.1:n.*1449A=
ENST00000367435.3:c.*943A=	ENSP00000356405.3:n.*943A=
NM_024529.4:c.*943A= , LRG_507t1:c.*943A=	NP_078805.3:n.*943A=
NM_024529.5:c.*943A= MANE Select	NP_078805.3:n.*943A=