Canonical Allele Identifier: CA422492640
Community Standard Title: NM_024529.5(CDC73):c.1560G>A (p.Arg520=)
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193250676G>A , CM000663.2:g.193250676G>A GRCh38
NC_000001.10:g.193219806G>A , CM000663.1:g.193219806G>A GRCh37
NC_000001.9:g.191486429G>A NCBI36
NG_012691.1:g.133719G>A , LRG_507:g.133719G>A

Transcript Alleles

HGVS Amino-acid Change
NM_024529.5:c.1560G>A MANE Select NP_078805.3:p.Arg520=
ENST00000367435.5:c.1560G>A MANE Select ENSP00000356405.4:p.Arg520=
NM_024529.4:c.1560G>A , LRG_507t1:c.1560G>A NP_078805.3:p.Arg520=
ENST00000367435.3:c.1560G>A ENSP00000356405.3:p.Arg520=
ENST00000477868.1:n.272G>A
ENST00000635846.1:c.1317G>A ENSP00000490035.1:p.Arg439=
ENST00000643006.1:c.*470G>A ENSP00000496633.1:n.*470G>A
ENST00000648071.1:c.*1536G>A ENSP00000497513.1:n.*1536G>A
ENST00000649613.1:n.810G>A
ENST00000650197.1:c.*258G>A ENSP00000496929.1:n.*258G>A