Canonical Allele Identifier: CA1216171028

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251478G= , CM000663.2:g.193251478G=	GRCh38
NC_000001.10:g.193220608G= , CM000663.1:g.193220608G=	GRCh37
NC_000001.9:g.191487231G=	NCBI36
NG_012691.1:g.134521G= , LRG_507:g.134521G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*766G= MANE Select	ENSP00000356405.4:n.*766G=
ENST00000635846.1:c.*766G=	ENSP00000490035.1:n.*766G=
ENST00000643006.1:c.*1272G=	ENSP00000496633.1:n.*1272G=
ENST00000367435.3:c.*766G=	ENSP00000356405.3:n.*766G=
NM_024529.4:c.*766G= , LRG_507t1:c.*766G=	NP_078805.3:n.*766G=
NM_024529.5:c.*766G= MANE Select	NP_078805.3:n.*766G=