Canonical Allele Identifier: CA422348666
Gene: CDC73 HGNC NCBI

Linked Data

COSMIC: COSM133829
MyVariant Identifiers: chr1:g.193091362del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122232del , CM000663.2:g.193122232del GRCh38
NC_000001.10:g.193091362del , CM000663.1:g.193091362del GRCh37
NC_000001.9:g.191357985del NCBI36
NG_012691.1:g.5275del , LRG_507:g.5275del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.32del MANE Select ENSP00000356405.4:p.Tyr11SerfsTer10
ENST00000635846.1:c.32del ENSP00000490035.1:p.Tyr11SerfsTer10
ENST00000643006.1:c.32del ENSP00000496633.1:p.Tyr11SerfsTer10
ENST00000643784.1:c.32del ENSP00000494944.1:p.Tyr11SerfsTer10
ENST00000648071.1:c.32del ENSP00000497513.1:p.Tyr11SerfsTer10
ENST00000649606.1:n.45del
ENST00000649895.1:n.250del
ENST00000650197.1:c.32del ENSP00000496929.1:p.Tyr11SerfsTer10
ENST00000367435.3:c.32del ENSP00000356405.3:p.Tyr11SerfsTer10
NM_024529.4:c.32del , LRG_507t1:c.32del NP_078805.3:p.Tyr11SerfsTer10
XM_006711537.2:c.32del XP_006711600.1:p.Tyr11SerfsTer10
XM_006711537.4:c.32del XP_006711600.1:p.Tyr11SerfsTer10
XR_001738350.1:n.1425del
NM_024529.5:c.32del MANE Select NP_078805.3:p.Tyr11SerfsTer10