Canonical Allele Identifier: CA2580061746

Gene: CDC73

Linked Data

• ClinVar Variation Id: 2006851
• ClinVar RCV Id: RCV002837949

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203866A>C , CM000663.2:g.193203866A>C	GRCh38
NC_000001.10:g.193172996A>C , CM000663.1:g.193172996A>C	GRCh37
NC_000001.9:g.191439619A>C	NCBI36
NG_012691.1:g.86909A>C , LRG_507:g.86909A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+14A>C MANE Select	ENSP00000356405.4:n.1030+14A>C
ENST00000635846.1:c.787+14A>C	ENSP00000490035.1:n.787+14A>C
ENST00000643006.1:c.1098+14A>C	ENSP00000496633.1:n.1098+14A>C
ENST00000648071.1:c.*1006+14A>C	ENSP00000497513.1:n.*1006+14A>C
ENST00000649613.1:n.280+14A>C
ENST00000649895.1:n.1248+14A>C
ENST00000650197.1:c.1030+14A>C	ENSP00000496929.1:n.1030+14A>C
ENST00000367435.3:c.1030+14A>C	ENSP00000356405.3:n.1030+14A>C
NM_024529.4:c.1030+14A>C , LRG_507t1:c.1030+14A>C	NP_078805.3:n.1030+14A>C
NM_024529.5:c.1030+14A>C MANE Select	NP_078805.3:n.1030+14A>C