Canonical Allele Identifier: CA1216171179
Gene: CDC73 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251840C= , CM000663.2:g.193251840C= GRCh38
NC_000001.10:g.193220970C= , CM000663.1:g.193220970C= GRCh37
NC_000001.9:g.191487593C= NCBI36
NG_012691.1:g.134883C= , LRG_507:g.134883C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1128C= MANE Select ENSP00000356405.4:n.*1128C=
ENST00000635846.1:c.*1128C= ENSP00000490035.1:n.*1128C=
ENST00000643006.1:c.*1634C= ENSP00000496633.1:n.*1634C=
ENST00000367435.3:c.*1128C= ENSP00000356405.3:n.*1128C=
NM_024529.4:c.*1128C= , LRG_507t1:c.*1128C= NP_078805.3:n.*1128C=
NM_024529.5:c.*1128C= MANE Select NP_078805.3:n.*1128C=
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