Canonical Allele Identifier: CA1216171172
Gene: CDC73 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251811G= , CM000663.2:g.193251811G= GRCh38
NC_000001.10:g.193220941G= , CM000663.1:g.193220941G= GRCh37
NC_000001.9:g.191487564G= NCBI36
NG_012691.1:g.134854G= , LRG_507:g.134854G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1099G= MANE Select ENSP00000356405.4:n.*1099G=
ENST00000635846.1:c.*1099G= ENSP00000490035.1:n.*1099G=
ENST00000643006.1:c.*1605G= ENSP00000496633.1:n.*1605G=
ENST00000367435.3:c.*1099G= ENSP00000356405.3:n.*1099G=
NM_024529.4:c.*1099G= , LRG_507t1:c.*1099G= NP_078805.3:n.*1099G=
NM_024529.5:c.*1099G= MANE Select NP_078805.3:n.*1099G=
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