Canonical Allele Identifier: CA2649631127
Gene: CDC73 HGNC NCBI

Linked Data

gnomAD v4: 1-193252004-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193252004C>A , CM000663.2:g.193252004C>A GRCh38
NC_000001.10:g.193221134C>A , CM000663.1:g.193221134C>A GRCh37
NC_000001.9:g.191487757C>A NCBI36
NG_012691.1:g.135047C>A , LRG_507:g.135047C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1292C>A MANE Select ENSP00000356405.4:n.*1292C>A
ENST00000635846.1:c.*1292C>A ENSP00000490035.1:n.*1292C>A
ENST00000643006.1:c.*1798C>A ENSP00000496633.1:n.*1798C>A
ENST00000367435.3:c.*1292C>A ENSP00000356405.3:n.*1292C>A
NM_024529.4:c.*1292C>A , LRG_507t1:c.*1292C>A NP_078805.3:n.*1292C>A
NM_024529.5:c.*1292C>A MANE Select NP_078805.3:n.*1292C>A
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