Canonical Allele Identifier: CA1216113346
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1675459230

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122140_193122142del , CM000663.2:g.193122140_193122142del GRCh38
NC_000001.10:g.193091270_193091272del , CM000663.1:g.193091270_193091272del GRCh37
NC_000001.9:g.191357893_191357895del NCBI36
NG_012691.1:g.5183_5185del , LRG_507:g.5183_5185del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-61_-59del MANE Select ENSP00000356405.4:n.-61_-59del
ENST00000643006.1:c.-61_-59del ENSP00000496633.1:n.-61_-59del
ENST00000643784.1:c.-61_-59del ENSP00000494944.1:n.-61_-59del
ENST00000649895.1:n.158_160del
ENST00000650197.1:c.-61_-59del ENSP00000496929.1:n.-61_-59del
ENST00000367435.3:c.-61_-59del ENSP00000356405.3:n.-61_-59del
NM_024529.4:c.-61_-59del , LRG_507t1:c.-61_-59del NP_078805.3:n.-61_-59del
XM_006711537.2:c.-61_-59del XP_006711600.1:n.-61_-59del
XM_006711537.4:c.-61_-59del XP_006711600.1:n.-61_-59del
XR_001738350.1:n.1520_1522del
NM_024529.5:c.-61_-59del MANE Select NP_078805.3:n.-61_-59del