Canonical Allele Identifier: CA1216171197

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251871A= , CM000663.2:g.193251871A=	GRCh38
NC_000001.10:g.193221001A= , CM000663.1:g.193221001A=	GRCh37
NC_000001.9:g.191487624A=	NCBI36
NG_012691.1:g.134914A= , LRG_507:g.134914A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*1159A= MANE Select	ENSP00000356405.4:n.*1159A=
ENST00000635846.1:c.*1159A=	ENSP00000490035.1:n.*1159A=
ENST00000643006.1:c.*1665A=	ENSP00000496633.1:n.*1665A=
ENST00000367435.3:c.*1159A=	ENSP00000356405.3:n.*1159A=
NM_024529.4:c.*1159A= , LRG_507t1:c.*1159A=	NP_078805.3:n.*1159A=
NM_024529.5:c.*1159A= MANE Select	NP_078805.3:n.*1159A=