Canonical Allele Identifier: CA2649598715
Gene: CDC73 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203705del , CM000663.2:g.193203705del GRCh38
NC_000001.10:g.193172835del , CM000663.1:g.193172835del GRCh37
NC_000001.9:g.191439458del NCBI36
NG_012691.1:g.86748del , LRG_507:g.86748del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.973-90del MANE Select ENSP00000356405.4:n.973-90del
ENST00000635846.1:c.730-90del ENSP00000490035.1:n.730-90del
ENST00000643006.1:c.1041-90del ENSP00000496633.1:n.1041-90del
ENST00000648071.1:c.*949-90del ENSP00000497513.1:n.*949-90del
ENST00000649613.1:n.223-90del
ENST00000649895.1:n.1191-90del
ENST00000650197.1:c.973-90del ENSP00000496929.1:n.973-90del
ENST00000367435.3:c.973-90del ENSP00000356405.3:n.973-90del
NM_024529.4:c.973-90del , LRG_507t1:c.973-90del NP_078805.3:n.973-90del
NM_024529.5:c.973-90del MANE Select NP_078805.3:n.973-90del