Canonical Allele Identifier: CA422345217

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193111161_193111162insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142033dup , CM000663.2:g.193142033dup	GRCh38
NC_000001.10:g.193111163dup , CM000663.1:g.193111163dup	GRCh37
NC_000001.9:g.191377786dup	NCBI36
NG_012691.1:g.25076dup , LRG_507:g.25076dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.696dup MANE Select	ENSP00000356405.4:p.Thr233AspfsTer?
ENST00000635846.1:c.696dup	ENSP00000490035.1:p.Thr233AspfsTer?
ENST00000643006.1:c.696dup	ENSP00000496633.1:p.Thr233AspfsTer?
ENST00000643784.1:c.*172dup	ENSP00000494944.1:n.*172dup
ENST00000647662.1:n.597dup
ENST00000648071.1:c.*672dup	ENSP00000497513.1:n.*672dup
ENST00000649606.1:n.709dup
ENST00000649895.1:n.914dup
ENST00000650197.1:c.696dup	ENSP00000496929.1:p.Thr233AspfsTer?
ENST00000367435.3:c.696dup	ENSP00000356405.3:p.Thr233AspfsTer?
NM_024529.4:c.696dup , LRG_507t1:c.696dup	NP_078805.3:p.Thr233AspfsTer?
XM_006711537.2:c.696dup	XP_006711600.1:p.Thr233AspfsTer?
XM_006711537.4:c.696dup	XP_006711600.1:p.Thr233AspfsTer?
NM_024529.5:c.696dup MANE Select	NP_078805.3:p.Thr233AspfsTer?