Canonical Allele Identifier: CA2697554802

Gene: CDC73

Linked Data

• ClinVar Variation Id: 2748058
• ClinVar RCV Id: RCV003501976

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122269_193122270delinsTT , CM000663.2:g.193122269_193122270delinsTT	GRCh38
NC_000001.10:g.193091399_193091400delinsTT , CM000663.1:g.193091399_193091400delinsTT	GRCh37
NC_000001.9:g.191358022_191358023delinsTT	NCBI36
NG_012691.1:g.5312_5313delinsTT , LRG_507:g.5312_5313delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.69_70delinsTT MANE Select	ENSP00000356405.4:p.Asp24Ter
ENST00000635846.1:c.69_70delinsTT	ENSP00000490035.1:p.Asp24Ter
ENST00000643006.1:c.69_70delinsTT	ENSP00000496633.1:p.Asp24Ter
ENST00000643784.1:c.69_70delinsTT	ENSP00000494944.1:p.Asp24Ter
ENST00000648071.1:c.69_70delinsTT	ENSP00000497513.1:p.Asp24Ter
ENST00000649606.1:n.82_83delinsTT
ENST00000649895.1:n.287_288delinsTT
ENST00000650197.1:c.69_70delinsTT	ENSP00000496929.1:p.Asp24Ter
ENST00000367435.3:c.69_70delinsTT	ENSP00000356405.3:p.Asp24Ter
NM_024529.4:c.69_70delinsTT , LRG_507t1:c.69_70delinsTT	NP_078805.3:p.Asp24Ter
XM_006711537.2:c.69_70delinsTT	XP_006711600.1:p.Asp24Ter
XM_006711537.4:c.69_70delinsTT	XP_006711600.1:p.Asp24Ter
XR_001738350.1:n.1387_1388delinsAA
NM_024529.5:c.69_70delinsTT MANE Select	NP_078805.3:p.Asp24Ter