Canonical Allele Identifier: CA343962708

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193111128A>C (hg19) ; chr1:g.193141998A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193141998A>C , CM000663.2:g.193141998A>C	GRCh38
NC_000001.10:g.193111128A>C , CM000663.1:g.193111128A>C	GRCh37
NC_000001.9:g.191377751A>C	NCBI36
NG_012691.1:g.25041A>C , LRG_507:g.25041A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.661A>C MANE Select	ENSP00000356405.4:p.Thr221Pro
ENST00000635846.1:c.661A>C	ENSP00000490035.1:p.Thr221Pro
ENST00000643006.1:c.661A>C	ENSP00000496633.1:p.Thr221Pro
ENST00000643784.1:c.*137A>C	ENSP00000494944.1:n.*137A>C
ENST00000647662.1:n.562A>C
ENST00000648071.1:c.*637A>C	ENSP00000497513.1:n.*637A>C
ENST00000649606.1:n.674A>C
ENST00000649895.1:n.879A>C
ENST00000650197.1:c.661A>C	ENSP00000496929.1:p.Thr221Pro
ENST00000367435.3:c.661A>C	ENSP00000356405.3:p.Thr221Pro
NM_024529.4:c.661A>C , LRG_507t1:c.661A>C	NP_078805.3:p.Thr221Pro
XM_006711537.2:c.661A>C	XP_006711600.1:p.Thr221Pro
XM_006711537.4:c.661A>C	XP_006711600.1:p.Thr221Pro
NM_024529.5:c.661A>C MANE Select	NP_078805.3:p.Thr221Pro