Canonical Allele Identifier: CA2649631098

Gene: CDC73

Linked Data

• gnomAD v4: 1-193251844-G-GTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251853_193251856dup , CM000663.2:g.193251853_193251856dup	GRCh38
NC_000001.10:g.193220983_193220986dup , CM000663.1:g.193220983_193220986dup	GRCh37
NC_000001.9:g.191487606_191487609dup	NCBI36
NG_012691.1:g.134896_134899dup , LRG_507:g.134896_134899dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*1141_*1144dup MANE Select	ENSP00000356405.4:n.*1141_*1144dup
ENST00000635846.1:c.*1141_*1144dup	ENSP00000490035.1:n.*1141_*1144dup
ENST00000643006.1:c.*1647_*1650dup	ENSP00000496633.1:n.*1647_*1650dup
ENST00000367435.3:c.*1141_*1144dup	ENSP00000356405.3:n.*1141_*1144dup
NM_024529.4:c.*1141_*1144dup , LRG_507t1:c.*1141_*1144dup	NP_078805.3:n.*1141_*1144dup
NM_024529.5:c.*1141_*1144dup MANE Select	NP_078805.3:n.*1141_*1144dup