Canonical Allele Identifier: CA2580061769

Gene: CDC73

Linked Data

• ClinVar Variation Id: 1932793
• ClinVar RCV Id: RCV002649513

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142076A>T , CM000663.2:g.193142076A>T	GRCh38
NC_000001.10:g.193111206A>T , CM000663.1:g.193111206A>T	GRCh37
NC_000001.9:g.191377829A>T	NCBI36
NG_012691.1:g.25119A>T , LRG_507:g.25119A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.729+10A>T MANE Select	ENSP00000356405.4:n.729+10A>T
ENST00000635846.1:c.729+10A>T	ENSP00000490035.1:n.729+10A>T
ENST00000643006.1:c.729+10A>T	ENSP00000496633.1:n.729+10A>T
ENST00000643784.1:c.*205+10A>T	ENSP00000494944.1:n.*205+10A>T
ENST00000647662.1:n.630+10A>T
ENST00000648071.1:c.*705+10A>T	ENSP00000497513.1:n.*705+10A>T
ENST00000649606.1:n.742+10A>T
ENST00000649895.1:n.947+10A>T
ENST00000650197.1:c.729+10A>T	ENSP00000496929.1:n.729+10A>T
ENST00000367435.3:c.729+10A>T	ENSP00000356405.3:n.729+10A>T
NM_024529.4:c.729+10A>T , LRG_507t1:c.729+10A>T	NP_078805.3:n.729+10A>T
XM_006711537.2:c.729+10A>T	XP_006711600.1:n.729+10A>T
XM_006711537.4:c.729+10A>T	XP_006711600.1:n.729+10A>T
NM_024529.5:c.729+10A>T MANE Select	NP_078805.3:n.729+10A>T