Canonical Allele Identifier: CA2697554806

Gene: CDC73

Linked Data

• ClinVar Variation Id: 2765330
• ClinVar RCV Id: RCV003500350

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142085T>G , CM000663.2:g.193142085T>G	GRCh38
NC_000001.10:g.193111215T>G , CM000663.1:g.193111215T>G	GRCh37
NC_000001.9:g.191377838T>G	NCBI36
NG_012691.1:g.25128T>G , LRG_507:g.25128T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.729+19T>G MANE Select	ENSP00000356405.4:n.729+19T>G
ENST00000635846.1:c.729+19T>G	ENSP00000490035.1:n.729+19T>G
ENST00000643006.1:c.729+19T>G	ENSP00000496633.1:n.729+19T>G
ENST00000643784.1:c.*205+19T>G	ENSP00000494944.1:n.*205+19T>G
ENST00000647662.1:n.630+19T>G
ENST00000648071.1:c.*705+19T>G	ENSP00000497513.1:n.*705+19T>G
ENST00000649606.1:n.742+19T>G
ENST00000649895.1:n.947+19T>G
ENST00000650197.1:c.729+19T>G	ENSP00000496929.1:n.729+19T>G
ENST00000367435.3:c.729+19T>G	ENSP00000356405.3:n.729+19T>G
NM_024529.4:c.729+19T>G , LRG_507t1:c.729+19T>G	NP_078805.3:n.729+19T>G
XM_006711537.2:c.729+19T>G	XP_006711600.1:n.729+19T>G
XM_006711537.4:c.729+19T>G	XP_006711600.1:n.729+19T>G
NM_024529.5:c.729+19T>G MANE Select	NP_078805.3:n.729+19T>G