Canonical Allele Identifier: CA1216171004
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251413C= , CM000663.2:g.193251413C= GRCh38
NC_000001.10:g.193220543C= , CM000663.1:g.193220543C= GRCh37
NC_000001.9:g.191487166C= NCBI36
NG_012691.1:g.134456C= , LRG_507:g.134456C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*701C= MANE Select ENSP00000356405.4:n.*701C=
ENST00000635846.1:c.*701C= ENSP00000490035.1:n.*701C=
ENST00000643006.1:c.*1207C= ENSP00000496633.1:n.*1207C=
ENST00000367435.3:c.*701C= ENSP00000356405.3:n.*701C=
NM_024529.4:c.*701C= , LRG_507t1:c.*701C= NP_078805.3:n.*701C=
NM_024529.5:c.*701C= MANE Select NP_078805.3:n.*701C=