Canonical Allele Identifier: CA1216171263
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193252003C= , CM000663.2:g.193252003C= GRCh38
NC_000001.10:g.193221133C= , CM000663.1:g.193221133C= GRCh37
NC_000001.9:g.191487756C= NCBI36
NG_012691.1:g.135046C= , LRG_507:g.135046C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1291C= MANE Select ENSP00000356405.4:n.*1291C=
ENST00000635846.1:c.*1291C= ENSP00000490035.1:n.*1291C=
ENST00000643006.1:c.*1797C= ENSP00000496633.1:n.*1797C=
ENST00000367435.3:c.*1291C= ENSP00000356405.3:n.*1291C=
NM_024529.4:c.*1291C= , LRG_507t1:c.*1291C= NP_078805.3:n.*1291C=
NM_024529.5:c.*1291C= MANE Select NP_078805.3:n.*1291C=