Canonical Allele Identifier: CA1216171024
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251466G= , CM000663.2:g.193251466G= GRCh38
NC_000001.10:g.193220596G= , CM000663.1:g.193220596G= GRCh37
NC_000001.9:g.191487219G= NCBI36
NG_012691.1:g.134509G= , LRG_507:g.134509G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*754G= MANE Select ENSP00000356405.4:n.*754G=
ENST00000635846.1:c.*754G= ENSP00000490035.1:n.*754G=
ENST00000643006.1:c.*1260G= ENSP00000496633.1:n.*1260G=
ENST00000367435.3:c.*754G= ENSP00000356405.3:n.*754G=
NM_024529.4:c.*754G= , LRG_507t1:c.*754G= NP_078805.3:n.*754G=
NM_024529.5:c.*754G= MANE Select NP_078805.3:n.*754G=