Canonical Allele Identifier: CA2580611522

Gene: CDC73

Linked Data

• ClinVar Variation Id: 2032515
• ClinVar RCV Id: RCV002884968

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122256_193122257del , CM000663.2:g.193122256_193122257del	GRCh38
NC_000001.10:g.193091386_193091387del , CM000663.1:g.193091386_193091387del	GRCh37
NC_000001.9:g.191358009_191358010del	NCBI36
NG_012691.1:g.5299_5300del , LRG_507:g.5299_5300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.56_57del MANE Select	ENSP00000356405.4:p.Val19GlyfsTer?
ENST00000635846.1:c.56_57del	ENSP00000490035.1:p.Val19GlyfsTer?
ENST00000643006.1:c.56_57del	ENSP00000496633.1:p.Val19GlyfsTer?
ENST00000643784.1:c.56_57del	ENSP00000494944.1:p.Val19GlyfsTer?
ENST00000648071.1:c.56_57del	ENSP00000497513.1:p.Val19GlyfsTer?
ENST00000649606.1:n.69_70del
ENST00000649895.1:n.274_275del
ENST00000650197.1:c.56_57del	ENSP00000496929.1:p.Val19GlyfsTer?
ENST00000367435.3:c.56_57del	ENSP00000356405.3:p.Val19GlyfsTer?
NM_024529.4:c.56_57del , LRG_507t1:c.56_57del	NP_078805.3:p.Val19GlyfsTer?
XM_006711537.2:c.56_57del	XP_006711600.1:p.Val19GlyfsTer?
XM_006711537.4:c.56_57del	XP_006711600.1:p.Val19GlyfsTer?
XR_001738350.1:n.1402_1403del
NM_024529.5:c.56_57del MANE Select	NP_078805.3:p.Val19GlyfsTer?