Canonical Allele Identifier: CA645522226

Gene: CDC73

Linked Data

• COSMIC: COSM26055

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142023_193142026del , CM000663.2:g.193142023_193142026del	GRCh38
NC_000001.10:g.193111153_193111156del , CM000663.1:g.193111153_193111156del	GRCh37
NC_000001.9:g.191377776_191377779del	NCBI36
NG_012691.1:g.25066_25069del , LRG_507:g.25066_25069del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.686_689del MANE Select	ENSP00000356405.4:p.Arg229AsnfsTer27
ENST00000635846.1:c.686_689del	ENSP00000490035.1:p.Arg229AsnfsTer?
ENST00000643006.1:c.686_689del	ENSP00000496633.1:p.Arg229AsnfsTer27
ENST00000643784.1:c.*162_*165del	ENSP00000494944.1:n.*162_*165del
ENST00000647662.1:n.587_590del
ENST00000648071.1:c.*662_*665del	ENSP00000497513.1:n.*662_*665del
ENST00000649606.1:n.699_702del
ENST00000649895.1:n.904_907del
ENST00000650197.1:c.686_689del	ENSP00000496929.1:p.Arg229AsnfsTer27
ENST00000367435.3:c.686_689del	ENSP00000356405.3:p.Arg229AsnfsTer27
NM_024529.4:c.686_689del , LRG_507t1:c.686_689del	NP_078805.3:p.Arg229AsnfsTer27
XM_006711537.2:c.686_689del	XP_006711600.1:p.Arg229AsnfsTer27
XM_006711537.4:c.686_689del	XP_006711600.1:p.Arg229AsnfsTer27
NM_024529.5:c.686_689del MANE Select	NP_078805.3:p.Arg229AsnfsTer27