Canonical Allele Identifier: CA2539406429
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251481del , CM000663.2:g.193251481del GRCh38
NC_000001.10:g.193220611del , CM000663.1:g.193220611del GRCh37
NC_000001.9:g.191487234del NCBI36
NG_012691.1:g.134524del , LRG_507:g.134524del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*769del MANE Select ENSP00000356405.4:n.*769del
ENST00000635846.1:c.*769del ENSP00000490035.1:n.*769del
ENST00000643006.1:c.*1275del ENSP00000496633.1:n.*1275del
ENST00000367435.3:c.*769del ENSP00000356405.3:n.*769del
NM_024529.4:c.*769del , LRG_507t1:c.*769del NP_078805.3:n.*769del
NM_024529.5:c.*769del MANE Select NP_078805.3:n.*769del