Canonical Allele Identifier: CA2580061770

Gene: CDC73

Linked Data

• ClinVar Variation Id: 1974558
• ClinVar RCV Id: RCV002741460

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142079T>C , CM000663.2:g.193142079T>C	GRCh38
NC_000001.10:g.193111209T>C , CM000663.1:g.193111209T>C	GRCh37
NC_000001.9:g.191377832T>C	NCBI36
NG_012691.1:g.25122T>C , LRG_507:g.25122T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.729+13T>C MANE Select	ENSP00000356405.4:n.729+13T>C
ENST00000635846.1:c.729+13T>C	ENSP00000490035.1:n.729+13T>C
ENST00000643006.1:c.729+13T>C	ENSP00000496633.1:n.729+13T>C
ENST00000643784.1:c.*205+13T>C	ENSP00000494944.1:n.*205+13T>C
ENST00000647662.1:n.630+13T>C
ENST00000648071.1:c.*705+13T>C	ENSP00000497513.1:n.*705+13T>C
ENST00000649606.1:n.742+13T>C
ENST00000649895.1:n.947+13T>C
ENST00000650197.1:c.729+13T>C	ENSP00000496929.1:n.729+13T>C
ENST00000367435.3:c.729+13T>C	ENSP00000356405.3:n.729+13T>C
NM_024529.4:c.729+13T>C , LRG_507t1:c.729+13T>C	NP_078805.3:n.729+13T>C
XM_006711537.2:c.729+13T>C	XP_006711600.1:n.729+13T>C
XM_006711537.4:c.729+13T>C	XP_006711600.1:n.729+13T>C
NM_024529.5:c.729+13T>C MANE Select	NP_078805.3:n.729+13T>C