Canonical Allele Identifier: CA422348809

Gene: CDC73

Linked Data

• COSMIC: COSM26052
• MyVariant Identifiers: chr1:g.193091406del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122276del , CM000663.2:g.193122276del	GRCh38
NC_000001.10:g.193091406del , CM000663.1:g.193091406del	GRCh37
NC_000001.9:g.191358029del	NCBI36
NG_012691.1:g.5319del , LRG_507:g.5319del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.76del MANE Select	ENSP00000356405.4:p.Ile26SerfsTer11
ENST00000635846.1:c.76del	ENSP00000490035.1:p.Ile26SerfsTer11
ENST00000643006.1:c.76del	ENSP00000496633.1:p.Ile26SerfsTer11
ENST00000643784.1:c.76del	ENSP00000494944.1:p.Ile26SerfsTer11
ENST00000648071.1:c.76del	ENSP00000497513.1:p.Ile26SerfsTer11
ENST00000649606.1:n.89del
ENST00000649895.1:n.294del
ENST00000650197.1:c.76del	ENSP00000496929.1:p.Ile26SerfsTer11
ENST00000367435.3:c.76del	ENSP00000356405.3:p.Ile26SerfsTer11
NM_024529.4:c.76del , LRG_507t1:c.76del	NP_078805.3:p.Ile26SerfsTer11
XM_006711537.2:c.76del	XP_006711600.1:p.Ile26SerfsTer11
XM_006711537.4:c.76del	XP_006711600.1:p.Ile26SerfsTer11
XR_001738350.1:n.1381del
NM_024529.5:c.76del MANE Select	NP_078805.3:p.Ile26SerfsTer11