Canonical Allele Identifier: CA1141540418
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251428A= , CM000663.2:g.193251428A= GRCh38
NC_000001.10:g.193220558A= , CM000663.1:g.193220558A= GRCh37
NC_000001.9:g.191487181A= NCBI36
NG_012691.1:g.134471A= , LRG_507:g.134471A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*716A= MANE Select ENSP00000356405.4:n.*716A=
ENST00000635846.1:c.*716A= ENSP00000490035.1:n.*716A=
ENST00000643006.1:c.*1222A= ENSP00000496633.1:n.*1222A=
ENST00000367435.3:c.*716A= ENSP00000356405.3:n.*716A=
NM_024529.4:c.*716A= , LRG_507t1:c.*716A= NP_078805.3:n.*716A=
NM_024529.5:c.*716A= MANE Select NP_078805.3:n.*716A=