Canonical Allele Identifier: CA658653585

Gene: CDC73

Linked Data

• dbSNP Id: rs1675915180
• PubMed: PMID:25363760

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142036_193142037dup , CM000663.2:g.193142036_193142037dup	GRCh38
NC_000001.10:g.193111166_193111167dup , CM000663.1:g.193111166_193111167dup	GRCh37
NC_000001.9:g.191377789_191377790dup	NCBI36
NG_012691.1:g.25079_25080dup , LRG_507:g.25079_25080dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.699_700dup MANE Select	ENSP00000356405.4:p.Arg234HisfsTer24
ENST00000635846.1:c.699_700dup	ENSP00000490035.1:p.Arg234HisfsTer?
ENST00000643006.1:c.699_700dup	ENSP00000496633.1:p.Arg234HisfsTer24
ENST00000643784.1:c.*175_*176dup	ENSP00000494944.1:n.*175_*176dup
ENST00000647662.1:n.600_601dup
ENST00000648071.1:c.*675_*676dup	ENSP00000497513.1:n.*675_*676dup
ENST00000649606.1:n.712_713dup
ENST00000649895.1:n.917_918dup
ENST00000650197.1:c.699_700dup	ENSP00000496929.1:p.Arg234HisfsTer24
ENST00000367435.3:c.699_700dup	ENSP00000356405.3:p.Arg234HisfsTer24
NM_024529.4:c.699_700dup , LRG_507t1:c.699_700dup	NP_078805.3:p.Arg234HisfsTer24
XM_006711537.2:c.699_700dup	XP_006711600.1:p.Arg234HisfsTer24
XM_006711537.4:c.699_700dup	XP_006711600.1:p.Arg234HisfsTer24
NM_024529.5:c.699_700dup MANE Select	NP_078805.3:p.Arg234HisfsTer24