Canonical Allele Identifier: CA2649598801

Gene: CDC73

Linked Data

• gnomAD v4: 1-193203971-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203971C>A , CM000663.2:g.193203971C>A	GRCh38
NC_000001.10:g.193173101C>A , CM000663.1:g.193173101C>A	GRCh37
NC_000001.9:g.191439724C>A	NCBI36
NG_012691.1:g.87014C>A , LRG_507:g.87014C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+119C>A MANE Select	ENSP00000356405.4:n.1030+119C>A
ENST00000635846.1:c.787+119C>A	ENSP00000490035.1:n.787+119C>A
ENST00000643006.1:c.1098+119C>A	ENSP00000496633.1:n.1098+119C>A
ENST00000648071.1:c.*1006+119C>A	ENSP00000497513.1:n.*1006+119C>A
ENST00000649613.1:n.280+119C>A
ENST00000649895.1:n.1248+119C>A
ENST00000650197.1:c.1030+119C>A	ENSP00000496929.1:n.1030+119C>A
ENST00000367435.3:c.1030+119C>A	ENSP00000356405.3:n.1030+119C>A
NM_024529.4:c.1030+119C>A , LRG_507t1:c.1030+119C>A	NP_078805.3:n.1030+119C>A
NM_024529.5:c.1030+119C>A MANE Select	NP_078805.3:n.1030+119C>A