Canonical Allele Identifier: CA1143549345
Gene: CDC73 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251795A= , CM000663.2:g.193251795A= GRCh38
NC_000001.10:g.193220925A= , CM000663.1:g.193220925A= GRCh37
NC_000001.9:g.191487548A= NCBI36
NG_012691.1:g.134838A= , LRG_507:g.134838A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367435.5:c.*1083A= MANE Select ENSP00000356405.4:n.*1083A=
ENST00000635846.1:c.*1083A= ENSP00000490035.1:n.*1083A=
ENST00000643006.1:c.*1589A= ENSP00000496633.1:n.*1589A=
ENST00000367435.3:c.*1083A= ENSP00000356405.3:n.*1083A=
NM_024529.4:c.*1083A= , LRG_507t1:c.*1083A= NP_078805.3:n.*1083A=
NM_024529.5:c.*1083A= MANE Select NP_078805.3:n.*1083A=
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