Canonical Allele Identifier: CA2586967895

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122220_193122224delinsCCCT , CM000663.2:g.193122220_193122224delinsCCCT	GRCh38
NC_000001.10:g.193091350_193091354delinsCCCT , CM000663.1:g.193091350_193091354delinsCCCT	GRCh37
NC_000001.9:g.191357973_191357977delinsCCCT	NCBI36
NG_012691.1:g.5263_5267delinsCCCT , LRG_507:g.5263_5267delinsCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.20_24delinsCCCT MANE Select	ENSP00000356405.4:p.Val7AlafsTer14
ENST00000635846.1:c.20_24delinsCCCT	ENSP00000490035.1:p.Val7AlafsTer14
ENST00000643006.1:c.20_24delinsCCCT	ENSP00000496633.1:p.Val7AlafsTer14
ENST00000643784.1:c.20_24delinsCCCT	ENSP00000494944.1:p.Val7AlafsTer14
ENST00000648071.1:c.20_24delinsCCCT	ENSP00000497513.1:p.Val7AlafsTer14
ENST00000649606.1:n.33_37delinsCCCT
ENST00000649895.1:n.238_242delinsCCCT
ENST00000650197.1:c.20_24delinsCCCT	ENSP00000496929.1:p.Val7AlafsTer14
ENST00000367435.3:c.20_24delinsCCCT	ENSP00000356405.3:p.Val7AlafsTer14
NM_024529.4:c.20_24delinsCCCT , LRG_507t1:c.20_24delinsCCCT	NP_078805.3:p.Val7AlafsTer14
XM_006711537.2:c.20_24delinsCCCT	XP_006711600.1:p.Val7AlafsTer14
XM_006711537.4:c.20_24delinsCCCT	XP_006711600.1:p.Val7AlafsTer14
XR_001738350.1:n.1433_1437delinsAGGG
NM_024529.5:c.20_24delinsCCCT MANE Select	NP_078805.3:p.Val7AlafsTer14