Canonical Allele Identifier: CA344076107

Gene: CDC73

Linked Data

• ClinVar Variation Id: 2497615
• ClinVar RCV Id: RCV003214070
• MyVariant Identifiers: chr1:g.193172940C>G (hg19) ; chr1:g.193203810C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203810C>G , CM000663.2:g.193203810C>G	GRCh38
NC_000001.10:g.193172940C>G , CM000663.1:g.193172940C>G	GRCh37
NC_000001.9:g.191439563C>G	NCBI36
NG_012691.1:g.86853C>G , LRG_507:g.86853C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.988C>G MANE Select	ENSP00000356405.4:p.Arg330Gly
ENST00000635846.1:c.745C>G	ENSP00000490035.1:p.Arg249Gly
ENST00000643006.1:c.1056C>G	ENSP00000496633.1:p.Pro352=
ENST00000648071.1:c.*964C>G	ENSP00000497513.1:n.*964C>G
ENST00000649613.1:n.238C>G
ENST00000649895.1:n.1206C>G
ENST00000650197.1:c.988C>G	ENSP00000496929.1:p.Arg330Gly
ENST00000367435.3:c.988C>G	ENSP00000356405.3:p.Arg330Gly
NM_024529.4:c.988C>G , LRG_507t1:c.988C>G	NP_078805.3:p.Arg330Gly
NM_024529.5:c.988C>G MANE Select	NP_078805.3:p.Arg330Gly