Canonical Allele Identifier: CA2541570301
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251525T>A , CM000663.2:g.193251525T>A GRCh38
NC_000001.10:g.193220655T>A , CM000663.1:g.193220655T>A GRCh37
NC_000001.9:g.191487278T>A NCBI36
NG_012691.1:g.134568T>A , LRG_507:g.134568T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*813T>A MANE Select ENSP00000356405.4:n.*813T>A
ENST00000635846.1:c.*813T>A ENSP00000490035.1:n.*813T>A
ENST00000643006.1:c.*1319T>A ENSP00000496633.1:n.*1319T>A
ENST00000367435.3:c.*813T>A ENSP00000356405.3:n.*813T>A
NM_024529.4:c.*813T>A , LRG_507t1:c.*813T>A NP_078805.3:n.*813T>A
NM_024529.5:c.*813T>A MANE Select NP_078805.3:n.*813T>A