Canonical Allele Identifier: CA1216171129
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251709T= , CM000663.2:g.193251709T= GRCh38
NC_000001.10:g.193220839T= , CM000663.1:g.193220839T= GRCh37
NC_000001.9:g.191487462T= NCBI36
NG_012691.1:g.134752T= , LRG_507:g.134752T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*997T= MANE Select ENSP00000356405.4:n.*997T=
ENST00000635846.1:c.*997T= ENSP00000490035.1:n.*997T=
ENST00000643006.1:c.*1503T= ENSP00000496633.1:n.*1503T=
ENST00000367435.3:c.*997T= ENSP00000356405.3:n.*997T=
NM_024529.4:c.*997T= , LRG_507t1:c.*997T= NP_078805.3:n.*997T=
NM_024529.5:c.*997T= MANE Select NP_078805.3:n.*997T=