Canonical Allele Identifier: CA343962809

Gene: CDC73

Linked Data

• dbSNP Id: rs2103126462
• MyVariant Identifiers: chr1:g.193111174C>G (hg19) ; chr1:g.193142044C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142044C>G , CM000663.2:g.193142044C>G	GRCh38
NC_000001.10:g.193111174C>G , CM000663.1:g.193111174C>G	GRCh37
NC_000001.9:g.191377797C>G	NCBI36
NG_012691.1:g.25087C>G , LRG_507:g.25087C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.707C>G MANE Select	ENSP00000356405.4:p.Thr236Ser
ENST00000635846.1:c.707C>G	ENSP00000490035.1:p.Thr236Ser
ENST00000643006.1:c.707C>G	ENSP00000496633.1:p.Thr236Ser
ENST00000643784.1:c.*183C>G	ENSP00000494944.1:n.*183C>G
ENST00000647662.1:n.608C>G
ENST00000648071.1:c.*683C>G	ENSP00000497513.1:n.*683C>G
ENST00000649606.1:n.720C>G
ENST00000649895.1:n.925C>G
ENST00000650197.1:c.707C>G	ENSP00000496929.1:p.Thr236Ser
ENST00000367435.3:c.707C>G	ENSP00000356405.3:p.Thr236Ser
NM_024529.4:c.707C>G , LRG_507t1:c.707C>G	NP_078805.3:p.Thr236Ser
XM_006711537.2:c.707C>G	XP_006711600.1:p.Thr236Ser
XM_006711537.4:c.707C>G	XP_006711600.1:p.Thr236Ser
NM_024529.5:c.707C>G MANE Select	NP_078805.3:p.Thr236Ser