Canonical Allele Identifier: CA2649631089
Gene: CDC73 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251822C>T , CM000663.2:g.193251822C>T GRCh38
NC_000001.10:g.193220952C>T , CM000663.1:g.193220952C>T GRCh37
NC_000001.9:g.191487575C>T NCBI36
NG_012691.1:g.134865C>T , LRG_507:g.134865C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1110C>T MANE Select ENSP00000356405.4:n.*1110C>T
ENST00000635846.1:c.*1110C>T ENSP00000490035.1:n.*1110C>T
ENST00000643006.1:c.*1616C>T ENSP00000496633.1:n.*1616C>T
ENST00000367435.3:c.*1110C>T ENSP00000356405.3:n.*1110C>T
NM_024529.4:c.*1110C>T , LRG_507t1:c.*1110C>T NP_078805.3:n.*1110C>T
NM_024529.5:c.*1110C>T MANE Select NP_078805.3:n.*1110C>T