Canonical Allele Identifier: CA1216171059

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251574C= , CM000663.2:g.193251574C=	GRCh38
NC_000001.10:g.193220704C= , CM000663.1:g.193220704C=	GRCh37
NC_000001.9:g.191487327C=	NCBI36
NG_012691.1:g.134617C= , LRG_507:g.134617C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*862C= MANE Select	ENSP00000356405.4:n.*862C=
ENST00000635846.1:c.*862C=	ENSP00000490035.1:n.*862C=
ENST00000643006.1:c.*1368C=	ENSP00000496633.1:n.*1368C=
ENST00000367435.3:c.*862C=	ENSP00000356405.3:n.*862C=
NM_024529.4:c.*862C= , LRG_507t1:c.*862C=	NP_078805.3:n.*862C=
NM_024529.5:c.*862C= MANE Select	NP_078805.3:n.*862C=