Canonical Allele Identifier: CA1216171010

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251434T= , CM000663.2:g.193251434T=	GRCh38
NC_000001.10:g.193220564T= , CM000663.1:g.193220564T=	GRCh37
NC_000001.9:g.191487187T=	NCBI36
NG_012691.1:g.134477T= , LRG_507:g.134477T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*722T= MANE Select	ENSP00000356405.4:n.*722T=
ENST00000635846.1:c.*722T=	ENSP00000490035.1:n.*722T=
ENST00000643006.1:c.*1228T=	ENSP00000496633.1:n.*1228T=
ENST00000367435.3:c.*722T=	ENSP00000356405.3:n.*722T=
NM_024529.4:c.*722T= , LRG_507t1:c.*722T=	NP_078805.3:n.*722T=
NM_024529.5:c.*722T= MANE Select	NP_078805.3:n.*722T=