Canonical Allele Identifier: CA1216150082
Gene: CDC73 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193204118A= , CM000663.2:g.193204118A= GRCh38
NC_000001.10:g.193173248A= , CM000663.1:g.193173248A= GRCh37
NC_000001.9:g.191439871A= NCBI36
NG_012691.1:g.87161A= , LRG_507:g.87161A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.1030+266A= MANE Select ENSP00000356405.4:n.1030+266A=
ENST00000635846.1:c.787+266A= ENSP00000490035.1:n.787+266A=
ENST00000643006.1:c.1098+266A= ENSP00000496633.1:n.1098+266A=
ENST00000648071.1:c.*1006+266A= ENSP00000497513.1:n.*1006+266A=
ENST00000649613.1:n.280+266A=
ENST00000649895.1:n.1248+266A=
ENST00000650197.1:c.1030+266A= ENSP00000496929.1:n.1030+266A=
ENST00000367435.3:c.1030+266A= ENSP00000356405.3:n.1030+266A=
NM_024529.4:c.1030+266A= , LRG_507t1:c.1030+266A= NP_078805.3:n.1030+266A=
NM_024529.5:c.1030+266A= MANE Select NP_078805.3:n.1030+266A=
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