Canonical Allele Identifier: CA1216149989
Gene: CDC73 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203856G= , CM000663.2:g.193203856G= GRCh38
NC_000001.10:g.193172986G= , CM000663.1:g.193172986G= GRCh37
NC_000001.9:g.191439609G= NCBI36
NG_012691.1:g.86899G= , LRG_507:g.86899G=

Transcript Alleles

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