Canonical Allele Identifier: CA2574103641
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203714_193203715del , CM000663.2:g.193203714_193203715del GRCh38
NC_000001.10:g.193172844_193172845del , CM000663.1:g.193172844_193172845del GRCh37
NC_000001.9:g.191439467_191439468del NCBI36
NG_012691.1:g.86757_86758del , LRG_507:g.86757_86758del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.973-81_973-80del MANE Select ENSP00000356405.4:n.973-81_973-80del
ENST00000635846.1:c.730-81_730-80del ENSP00000490035.1:n.730-81_730-80del
ENST00000643006.1:c.1041-81_1041-80del ENSP00000496633.1:n.1041-81_1041-80del
ENST00000648071.1:c.*949-81_*949-80del ENSP00000497513.1:n.*949-81_*949-80del
ENST00000649613.1:n.223-81_223-80del
ENST00000649895.1:n.1191-81_1191-80del
ENST00000650197.1:c.973-81_973-80del ENSP00000496929.1:n.973-81_973-80del
ENST00000367435.3:c.973-81_973-80del ENSP00000356405.3:n.973-81_973-80del
NM_024529.4:c.973-81_973-80del , LRG_507t1:c.973-81_973-80del NP_078805.3:n.973-81_973-80del
NM_024529.5:c.973-81_973-80del MANE Select NP_078805.3:n.973-81_973-80del