Canonical Allele Identifier: CA1216150080

Gene: CDC73

Linked Data

• dbSNP Id: rs1677137984

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193204114del , CM000663.2:g.193204114del	GRCh38
NC_000001.10:g.193173244del , CM000663.1:g.193173244del	GRCh37
NC_000001.9:g.191439867del	NCBI36
NG_012691.1:g.87157del , LRG_507:g.87157del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+262del MANE Select	ENSP00000356405.4:n.1030+262del
ENST00000635846.1:c.787+262del	ENSP00000490035.1:n.787+262del
ENST00000643006.1:c.1098+262del	ENSP00000496633.1:n.1098+262del
ENST00000648071.1:c.*1006+262del	ENSP00000497513.1:n.*1006+262del
ENST00000649613.1:n.280+262del
ENST00000649895.1:n.1248+262del
ENST00000650197.1:c.1030+262del	ENSP00000496929.1:n.1030+262del
ENST00000367435.3:c.1030+262del	ENSP00000356405.3:n.1030+262del
NM_024529.4:c.1030+262del , LRG_507t1:c.1030+262del	NP_078805.3:n.1030+262del
NM_024529.5:c.1030+262del MANE Select	NP_078805.3:n.1030+262del