Canonical Allele Identifier: CA1303765

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193212395C>T , CM000663.2:g.193212395C>T	GRCh38
NC_000001.10:g.193181525C>T , CM000663.1:g.193181525C>T	GRCh37
NC_000001.9:g.191448148C>T	NCBI36
NG_012691.1:g.95438C>T , LRG_507:g.95438C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.1072C>T MANE Select	NP_078805.3:p.Arg358Ter
ENST00000367435.5:c.1072C>T MANE Select	ENSP00000356405.4:p.Arg358Ter
NM_024529.4:c.1072C>T , LRG_507t1:c.1072C>T	NP_078805.3:p.Arg358Ter
ENST00000367435.3:c.1072C>T	ENSP00000356405.3:p.Arg358Ter
ENST00000635846.1:c.829C>T	ENSP00000490035.1:p.Arg277Ter
ENST00000643006.1:c.1140C>T	ENSP00000496633.1:p.Leu380=
ENST00000648071.1:c.*1048C>T	ENSP00000497513.1:n.*1048C>T
ENST00000649613.1:n.322C>T
ENST00000649895.1:n.1290C>T
ENST00000650197.1:c.1072C>T	ENSP00000496929.1:p.Arg358Ter