Canonical Allele Identifier: CA2649631011
Gene: CDC73 HGNC NCBI

Linked Data

gnomAD v4: 1-193251451-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251451T>G , CM000663.2:g.193251451T>G GRCh38
NC_000001.10:g.193220581T>G , CM000663.1:g.193220581T>G GRCh37
NC_000001.9:g.191487204T>G NCBI36
NG_012691.1:g.134494T>G , LRG_507:g.134494T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*739T>G MANE Select ENSP00000356405.4:n.*739T>G
ENST00000635846.1:c.*739T>G ENSP00000490035.1:n.*739T>G
ENST00000643006.1:c.*1245T>G ENSP00000496633.1:n.*1245T>G
ENST00000367435.3:c.*739T>G ENSP00000356405.3:n.*739T>G
NM_024529.4:c.*739T>G , LRG_507t1:c.*739T>G NP_078805.3:n.*739T>G
NM_024529.5:c.*739T>G MANE Select NP_078805.3:n.*739T>G
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