Canonical Allele Identifier: CA2649624627
Gene: CDC73 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122102_193122159del , CM000663.2:g.193122102_193122159del GRCh38
NC_000001.10:g.193091232_193091289del , CM000663.1:g.193091232_193091289del GRCh37
NC_000001.9:g.191357855_191357912del NCBI36
NG_012691.1:g.5145_5202del , LRG_507:g.5145_5202del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-99_-42del MANE Select ENSP00000356405.4:n.-99_-42del
ENST00000643006.1:c.-99_-42del ENSP00000496633.1:n.-99_-42del
ENST00000649895.1:n.120_177del
ENST00000367435.3:c.-99_-42del ENSP00000356405.3:n.-99_-42del
NM_024529.4:c.-99_-42del , LRG_507t1:c.-99_-42del NP_078805.3:n.-99_-42del
XM_006711537.2:c.-99_-42del XP_006711600.1:n.-99_-42del
XM_006711537.4:c.-99_-42del XP_006711600.1:n.-99_-42del
XR_001738350.1:n.1507_1564del
NM_024529.5:c.-99_-42del MANE Select NP_078805.3:n.-99_-42del