Canonical Allele Identifier: CA2574103666
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203949del , CM000663.2:g.193203949del GRCh38
NC_000001.10:g.193173079del , CM000663.1:g.193173079del GRCh37
NC_000001.9:g.191439702del NCBI36
NG_012691.1:g.86992del , LRG_507:g.86992del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.1030+97del MANE Select ENSP00000356405.4:n.1030+97del
ENST00000635846.1:c.787+97del ENSP00000490035.1:n.787+97del
ENST00000643006.1:c.1098+97del ENSP00000496633.1:n.1098+97del
ENST00000648071.1:c.*1006+97del ENSP00000497513.1:n.*1006+97del
ENST00000649613.1:n.280+97del
ENST00000649895.1:n.1248+97del
ENST00000650197.1:c.1030+97del ENSP00000496929.1:n.1030+97del
ENST00000367435.3:c.1030+97del ENSP00000356405.3:n.1030+97del
NM_024529.4:c.1030+97del , LRG_507t1:c.1030+97del NP_078805.3:n.1030+97del
NM_024529.5:c.1030+97del MANE Select NP_078805.3:n.1030+97del