Canonical Allele Identifier: CA343972852

Gene: CDC73

Linked Data

• ClinVar Variation Id: 2450592
• ClinVar RCV Id: RCV003177055
• MyVariant Identifiers: chr1:g.193091389T>G (hg19) ; chr1:g.193122259T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122259T>G , CM000663.2:g.193122259T>G	GRCh38
NC_000001.10:g.193091389T>G , CM000663.1:g.193091389T>G	GRCh37
NC_000001.9:g.191358012T>G	NCBI36
NG_012691.1:g.5302T>G , LRG_507:g.5302T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.59T>G MANE Select	ENSP00000356405.4:p.Val20Gly
ENST00000635846.1:c.59T>G	ENSP00000490035.1:p.Val20Gly
ENST00000643006.1:c.59T>G	ENSP00000496633.1:p.Val20Gly
ENST00000643784.1:c.59T>G	ENSP00000494944.1:p.Val20Gly
ENST00000648071.1:c.59T>G	ENSP00000497513.1:p.Val20Gly
ENST00000649606.1:n.72T>G
ENST00000649895.1:n.277T>G
ENST00000650197.1:c.59T>G	ENSP00000496929.1:p.Val20Gly
ENST00000367435.3:c.59T>G	ENSP00000356405.3:p.Val20Gly
NM_024529.4:c.59T>G , LRG_507t1:c.59T>G	NP_078805.3:p.Val20Gly
XM_006711537.2:c.59T>G	XP_006711600.1:p.Val20Gly
XM_006711537.4:c.59T>G	XP_006711600.1:p.Val20Gly
XR_001738350.1:n.1398A>C
NM_024529.5:c.59T>G MANE Select	NP_078805.3:p.Val20Gly