Canonical Allele Identifier: CA2649597917

Gene: CDC73

Linked Data

• gnomAD v4: 1-193141966-AGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193141970_193141972del , CM000663.2:g.193141970_193141972del	GRCh38
NC_000001.10:g.193111100_193111102del , CM000663.1:g.193111100_193111102del	GRCh37
NC_000001.9:g.191377723_191377725del	NCBI36
NG_012691.1:g.25013_25015del , LRG_507:g.25013_25015del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.633_635del MANE Select	ENSP00000356405.4:p.Arg211del
ENST00000635846.1:c.633_635del	ENSP00000490035.1:p.Arg211del
ENST00000643006.1:c.633_635del	ENSP00000496633.1:p.Arg211del
ENST00000643784.1:c.*109_*111del	ENSP00000494944.1:n.*109_*111del
ENST00000647662.1:n.534_536del
ENST00000648071.1:c.*609_*611del	ENSP00000497513.1:n.*609_*611del
ENST00000649606.1:n.646_648del
ENST00000649895.1:n.851_853del
ENST00000650197.1:c.633_635del	ENSP00000496929.1:p.Arg211del
ENST00000367435.3:c.633_635del	ENSP00000356405.3:p.Arg211del
NM_024529.4:c.633_635del , LRG_507t1:c.633_635del	NP_078805.3:p.Arg211del
XM_006711537.2:c.633_635del	XP_006711600.1:p.Arg211del
XM_006711537.4:c.633_635del	XP_006711600.1:p.Arg211del
NM_024529.5:c.633_635del MANE Select	NP_078805.3:p.Arg211del