Canonical Allele Identifier: CA2649631099

Gene: CDC73

Linked Data

• gnomAD v4: 1-193251854-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251854_193251855insC , CM000663.2:g.193251854_193251855insC	GRCh38
NC_000001.10:g.193220984_193220985insC , CM000663.1:g.193220984_193220985insC	GRCh37
NC_000001.9:g.191487607_191487608insC	NCBI36
NG_012691.1:g.134897_134898insC , LRG_507:g.134897_134898insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*1142_*1143insC MANE Select	ENSP00000356405.4:n.*1142_*1143insC
ENST00000635846.1:c.*1142_*1143insC	ENSP00000490035.1:n.*1142_*1143insC
ENST00000643006.1:c.*1648_*1649insC	ENSP00000496633.1:n.*1648_*1649insC
ENST00000367435.3:c.*1142_*1143insC	ENSP00000356405.3:n.*1142_*1143insC
NM_024529.4:c.*1142_*1143insC , LRG_507t1:c.*1142_*1143insC	NP_078805.3:n.*1142_*1143insC
NM_024529.5:c.*1142_*1143insC MANE Select	NP_078805.3:n.*1142_*1143insC