Canonical Allele Identifier: CA2747147003
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203490del , CM000663.2:g.193203490del GRCh38
NC_000001.10:g.193172620del , CM000663.1:g.193172620del GRCh37
NC_000001.9:g.191439243del NCBI36
NG_012691.1:g.86533del , LRG_507:g.86533del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.973-305del MANE Select ENSP00000356405.4:n.973-305del
ENST00000635846.1:c.730-305del ENSP00000490035.1:n.730-305del
ENST00000643006.1:c.1041-305del ENSP00000496633.1:n.1041-305del
ENST00000648071.1:c.*949-305del ENSP00000497513.1:n.*949-305del
ENST00000649613.1:n.223-305del
ENST00000649895.1:n.1191-305del
ENST00000650197.1:c.973-305del ENSP00000496929.1:n.973-305del
ENST00000367435.3:c.973-305del ENSP00000356405.3:n.973-305del
NM_024529.4:c.973-305del , LRG_507t1:c.973-305del NP_078805.3:n.973-305del
NM_024529.5:c.973-305del MANE Select NP_078805.3:n.973-305del