Canonical Allele Identifier: CA10608625

Gene: CDC73

Linked Data

• ClinVar Variation Id: 294412
• ClinVar RCV Id: RCV002374495 ; RCV000397786 ; RCV000344041 ; RCV000296231
• dbSNP Id: rs886045713
• MyVariant Identifiers: chr1:g.193111126T>C (hg19) ; chr1:g.193141996T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193141996T>C , CM000663.2:g.193141996T>C	GRCh38
NC_000001.10:g.193111126T>C , CM000663.1:g.193111126T>C	GRCh37
NC_000001.9:g.191377749T>C	NCBI36
NG_012691.1:g.25039T>C , LRG_507:g.25039T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.659T>C MANE Select	ENSP00000356405.4:p.Val220Ala
ENST00000635846.1:c.659T>C	ENSP00000490035.1:p.Val220Ala
ENST00000643006.1:c.659T>C	ENSP00000496633.1:p.Val220Ala
ENST00000643784.1:c.*135T>C	ENSP00000494944.1:n.*135T>C
ENST00000647662.1:n.560T>C
ENST00000648071.1:c.*635T>C	ENSP00000497513.1:n.*635T>C
ENST00000649606.1:n.672T>C
ENST00000649895.1:n.877T>C
ENST00000650197.1:c.659T>C	ENSP00000496929.1:p.Val220Ala
ENST00000367435.3:c.659T>C	ENSP00000356405.3:p.Val220Ala
NM_024529.4:c.659T>C , LRG_507t1:c.659T>C	NP_078805.3:p.Val220Ala
XM_006711537.2:c.659T>C	XP_006711600.1:p.Val220Ala
XM_006711537.4:c.659T>C	XP_006711600.1:p.Val220Ala
NM_024529.5:c.659T>C MANE Select	NP_078805.3:p.Val220Ala