Canonical Allele Identifier: CA10581759

Gene: CDC73

Linked Data

• ClinVar Variation Id: 241493
• ClinVar RCV Id: RCV000234594 ; RCV003165647
• dbSNP Id: rs878855089
• gnomAD v3: 1-193122335-A-G
• gnomAD v4: 1-193122335-A-G
• MyVariant Identifiers: chr1:g.193091465A>G (hg19) ; chr1:g.193122335A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122335A>G , CM000663.2:g.193122335A>G	GRCh38
NC_000001.10:g.193091465A>G , CM000663.1:g.193091465A>G	GRCh37
NC_000001.9:g.191358088A>G	NCBI36
NG_012691.1:g.5378A>G , LRG_507:g.5378A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.131+4A>G MANE Select	ENSP00000356405.4:n.131+4A>G
ENST00000635846.1:c.131+4A>G	ENSP00000490035.1:n.131+4A>G
ENST00000643006.1:c.131+4A>G	ENSP00000496633.1:n.131+4A>G
ENST00000643784.1:c.131+4A>G	ENSP00000494944.1:n.131+4A>G
ENST00000647662.1:n.32+4A>G
ENST00000648071.1:c.131+4A>G	ENSP00000497513.1:n.131+4A>G
ENST00000649606.1:n.144+4A>G
ENST00000649895.1:n.349+4A>G
ENST00000650197.1:c.131+4A>G	ENSP00000496929.1:n.131+4A>G
ENST00000367435.3:c.131+4A>G	ENSP00000356405.3:n.131+4A>G
NM_024529.4:c.131+4A>G , LRG_507t1:c.131+4A>G	NP_078805.3:n.131+4A>G
XM_006711537.2:c.131+4A>G	XP_006711600.1:n.131+4A>G
XM_006711537.4:c.131+4A>G	XP_006711600.1:n.131+4A>G
XR_001738350.1:n.1322T>C
NM_024529.5:c.131+4A>G MANE Select	NP_078805.3:n.131+4A>G