Canonical Allele Identifier: CA1216171039

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251504T= , CM000663.2:g.193251504T=	GRCh38
NC_000001.10:g.193220634T= , CM000663.1:g.193220634T=	GRCh37
NC_000001.9:g.191487257T=	NCBI36
NG_012691.1:g.134547T= , LRG_507:g.134547T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*792T= MANE Select	ENSP00000356405.4:n.*792T=
ENST00000635846.1:c.*792T=	ENSP00000490035.1:n.*792T=
ENST00000643006.1:c.*1298T=	ENSP00000496633.1:n.*1298T=
ENST00000367435.3:c.*792T=	ENSP00000356405.3:n.*792T=
NM_024529.4:c.*792T= , LRG_507t1:c.*792T=	NP_078805.3:n.*792T=
NM_024529.5:c.*792T= MANE Select	NP_078805.3:n.*792T=