Canonical Allele Identifier: CA2739275473

Gene: CDC73

Linked Data

• ClinVar Variation Id: 2915842
• ClinVar RCV Id: RCV003607141

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193135375C>G , CM000663.2:g.193135375C>G	GRCh38
NC_000001.10:g.193104505C>G , CM000663.1:g.193104505C>G	GRCh37
NC_000001.9:g.191371128C>G	NCBI36
NG_012691.1:g.18418C>G , LRG_507:g.18418C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.308-16C>G MANE Select	ENSP00000356405.4:n.308-16C>G
ENST00000635846.1:c.308-16C>G	ENSP00000490035.1:n.308-16C>G
ENST00000643006.1:c.308-16C>G	ENSP00000496633.1:n.308-16C>G
ENST00000643784.1:c.308-16C>G	ENSP00000494944.1:n.308-16C>G
ENST00000647662.1:n.209-16C>G
ENST00000648071.1:c.*284-16C>G	ENSP00000497513.1:n.*284-16C>G
ENST00000649606.1:n.321-16C>G
ENST00000649706.1:n.249-16C>G
ENST00000649895.1:n.526-16C>G
ENST00000650197.1:c.308-16C>G	ENSP00000496929.1:n.308-16C>G
ENST00000367435.3:c.308-16C>G	ENSP00000356405.3:n.308-16C>G
ENST00000482484.1:n.560-16C>G
NM_024529.4:c.308-16C>G , LRG_507t1:c.308-16C>G	NP_078805.3:n.308-16C>G
XM_006711537.2:c.308-16C>G	XP_006711600.1:n.308-16C>G
XM_006711537.4:c.308-16C>G	XP_006711600.1:n.308-16C>G
NM_024529.5:c.308-16C>G MANE Select	NP_078805.3:n.308-16C>G