Canonical Allele Identifier: CA2649624652
Gene: CDC73 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122116_193122121del , CM000663.2:g.193122116_193122121del GRCh38
NC_000001.10:g.193091246_193091251del , CM000663.1:g.193091246_193091251del GRCh37
NC_000001.9:g.191357869_191357874del NCBI36
NG_012691.1:g.5159_5164del , LRG_507:g.5159_5164del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-85_-80del MANE Select ENSP00000356405.4:n.-85_-80del
ENST00000643006.1:c.-85_-80del ENSP00000496633.1:n.-85_-80del
ENST00000649895.1:n.134_139del
ENST00000650197.1:c.-85_-80del ENSP00000496929.1:n.-85_-80del
ENST00000367435.3:c.-85_-80del ENSP00000356405.3:n.-85_-80del
NM_024529.4:c.-85_-80del , LRG_507t1:c.-85_-80del NP_078805.3:n.-85_-80del
XM_006711537.2:c.-85_-80del XP_006711600.1:n.-85_-80del
XM_006711537.4:c.-85_-80del XP_006711600.1:n.-85_-80del
XR_001738350.1:n.1540_1545del
NM_024529.5:c.-85_-80del MANE Select NP_078805.3:n.-85_-80del