Canonical Allele Identifier: CA1216113435

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122281_193122282delinsCG , CM000663.2:g.193122281_193122282delinsCG	GRCh38
NC_000001.10:g.193091411_193091412delinsCG , CM000663.1:g.193091411_193091412delinsCG	GRCh37
NC_000001.9:g.191358034_191358035delinsCG	NCBI36
NG_012691.1:g.5324_5325delinsCG , LRG_507:g.5324_5325delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.81_82delinsCG MANE Select	ENSP00000356405.4:p.Phe27=
ENST00000635846.1:c.81_82delinsCG	ENSP00000490035.1:p.Phe27=
ENST00000643006.1:c.81_82delinsCG	ENSP00000496633.1:p.Phe27=
ENST00000643784.1:c.81_82delinsCG	ENSP00000494944.1:p.Phe27=
ENST00000648071.1:c.81_82delinsCG	ENSP00000497513.1:p.Phe27=
ENST00000649606.1:n.94_95delinsCG
ENST00000649895.1:n.299_300delinsCG
ENST00000650197.1:c.81_82delinsCG	ENSP00000496929.1:p.Phe27=
ENST00000367435.3:c.81_82delinsCG	ENSP00000356405.3:p.Phe27=
NM_024529.4:c.81_82delinsCG , LRG_507t1:c.81_82delinsCG	NP_078805.3:p.Phe27=
XM_006711537.2:c.81_82delinsCG	XP_006711600.1:p.Phe27=
XM_006711537.4:c.81_82delinsCG	XP_006711600.1:p.Phe27=
XR_001738350.1:n.1375_1376delinsCG
NM_024529.5:c.81_82delinsCG MANE Select	NP_078805.3:p.Phe27=