Canonical Allele Identifier: CA2649626285

Gene: CDC73

Linked Data

• ClinVar Variation Id: 2973962
• ClinVar RCV Id: RCV003833536
• gnomAD v4: 1-193130258-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193130258A>G , CM000663.2:g.193130258A>G	GRCh38
NC_000001.10:g.193099388A>G , CM000663.1:g.193099388A>G	GRCh37
NC_000001.9:g.191366011A>G	NCBI36
NG_012691.1:g.13301A>G , LRG_507:g.13301A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.307+15A>G MANE Select	ENSP00000356405.4:n.307+15A>G
ENST00000635846.1:c.307+15A>G	ENSP00000490035.1:n.307+15A>G
ENST00000643006.1:c.307+15A>G	ENSP00000496633.1:n.307+15A>G
ENST00000643784.1:c.307+15A>G	ENSP00000494944.1:n.307+15A>G
ENST00000647662.1:n.208+15A>G
ENST00000648071.1:c.*283+15A>G	ENSP00000497513.1:n.*283+15A>G
ENST00000649606.1:n.320+15A>G
ENST00000649706.1:n.248+15A>G
ENST00000649895.1:n.525+15A>G
ENST00000650197.1:c.307+15A>G	ENSP00000496929.1:n.307+15A>G
ENST00000367435.3:c.307+15A>G	ENSP00000356405.3:n.307+15A>G
ENST00000482484.1:n.559+15A>G
NM_024529.4:c.307+15A>G , LRG_507t1:c.307+15A>G	NP_078805.3:n.307+15A>G
XM_006711537.2:c.307+15A>G	XP_006711600.1:n.307+15A>G
XR_241165.2:n.303+99T>C
XM_006711537.4:c.307+15A>G	XP_006711600.1:n.307+15A>G
NM_024529.5:c.307+15A>G MANE Select	NP_078805.3:n.307+15A>G