Canonical Allele Identifier: CA2739275501

Gene: CDC73

Linked Data

• ClinVar Variation Id: 2840999
• ClinVar RCV Id: RCV003608176

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193130164T>G , CM000663.2:g.193130164T>G	GRCh38
NC_000001.10:g.193099294T>G , CM000663.1:g.193099294T>G	GRCh37
NC_000001.9:g.191365917T>G	NCBI36
NG_012691.1:g.13207T>G , LRG_507:g.13207T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.238-10T>G MANE Select	ENSP00000356405.4:n.238-10T>G
ENST00000635846.1:c.238-10T>G	ENSP00000490035.1:n.238-10T>G
ENST00000643006.1:c.238-10T>G	ENSP00000496633.1:n.238-10T>G
ENST00000643784.1:c.238-10T>G	ENSP00000494944.1:n.238-10T>G
ENST00000647662.1:n.139-10T>G
ENST00000648071.1:c.*214-10T>G	ENSP00000497513.1:n.*214-10T>G
ENST00000649606.1:n.251-10T>G
ENST00000649706.1:n.179-10T>G
ENST00000649895.1:n.456-10T>G
ENST00000650197.1:c.238-10T>G	ENSP00000496929.1:n.238-10T>G
ENST00000367435.3:c.238-10T>G	ENSP00000356405.3:n.238-10T>G
ENST00000482484.1:n.490-10T>G
NM_024529.4:c.238-10T>G , LRG_507t1:c.238-10T>G	NP_078805.3:n.238-10T>G
XM_006711537.2:c.238-10T>G	XP_006711600.1:n.238-10T>G
XR_241165.2:n.303+193A>C
XM_006711537.4:c.238-10T>G	XP_006711600.1:n.238-10T>G
NM_024529.5:c.238-10T>G MANE Select	NP_078805.3:n.238-10T>G