Canonical Allele Identifier: CA1216150069

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193204094_193204098delinsCATAA , CM000663.2:g.193204094_193204098delinsCATAA	GRCh38
NC_000001.10:g.193173224_193173228delinsCATAA , CM000663.1:g.193173224_193173228delinsCATAA	GRCh37
NC_000001.9:g.191439847_191439851delinsCATAA	NCBI36
NG_012691.1:g.87137_87141delinsCATAA , LRG_507:g.87137_87141delinsCATAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+242_1030+246delinsCATAA MANE Select	ENSP00000356405.4:n.1030+242_1030+246delinsCATAA
ENST00000635846.1:c.787+242_787+246delinsCATAA	ENSP00000490035.1:n.787+242_787+246delinsCATAA
ENST00000643006.1:c.1098+242_1098+246delinsCATAA	ENSP00000496633.1:n.1098+242_1098+246delinsCATAA
ENST00000648071.1:c.*1006+242_*1006+246delinsCATAA	ENSP00000497513.1:n.*1006+242_*1006+246delinsCATAA
ENST00000649613.1:n.280+242_280+246delinsCATAA
ENST00000649895.1:n.1248+242_1248+246delinsCATAA
ENST00000650197.1:c.1030+242_1030+246delinsCATAA	ENSP00000496929.1:n.1030+242_1030+246delinsCATAA
ENST00000367435.3:c.1030+242_1030+246delinsCATAA	ENSP00000356405.3:n.1030+242_1030+246delinsCATAA
NM_024529.4:c.1030+242_1030+246delinsCATAA , LRG_507t1:c.1030+242_1030+246delinsCATAA	NP_078805.3:n.1030+242_1030+246delinsCATAA
NM_024529.5:c.1030+242_1030+246delinsCATAA MANE Select	NP_078805.3:n.1030+242_1030+246delinsCATAA