Canonical Allele Identifier: CA1216171013
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1678041407

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251440_193251441del , CM000663.2:g.193251440_193251441del GRCh38
NC_000001.10:g.193220570_193220571del , CM000663.1:g.193220570_193220571del GRCh37
NC_000001.9:g.191487193_191487194del NCBI36
NG_012691.1:g.134483_134484del , LRG_507:g.134483_134484del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*728_*729del MANE Select ENSP00000356405.4:n.*728_*729del
ENST00000635846.1:c.*728_*729del ENSP00000490035.1:n.*728_*729del
ENST00000643006.1:c.*1234_*1235del ENSP00000496633.1:n.*1234_*1235del
ENST00000367435.3:c.*728_*729del ENSP00000356405.3:n.*728_*729del
NM_024529.4:c.*728_*729del , LRG_507t1:c.*728_*729del NP_078805.3:n.*728_*729del
NM_024529.5:c.*728_*729del MANE Select NP_078805.3:n.*728_*729del