Canonical Allele Identifier: CA422345168

Gene: CDC73

Linked Data

• dbSNP Id: rs2103126329
• MyVariant Identifiers: chr1:g.193111130C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142000C>G , CM000663.2:g.193142000C>G	GRCh38
NC_000001.10:g.193111130C>G , CM000663.1:g.193111130C>G	GRCh37
NC_000001.9:g.191377753C>G	NCBI36
NG_012691.1:g.25043C>G , LRG_507:g.25043C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.663C>G MANE Select	ENSP00000356405.4:p.Thr221=
ENST00000635846.1:c.663C>G	ENSP00000490035.1:p.Thr221=
ENST00000643006.1:c.663C>G	ENSP00000496633.1:p.Thr221=
ENST00000643784.1:c.*139C>G	ENSP00000494944.1:n.*139C>G
ENST00000647662.1:n.564C>G
ENST00000648071.1:c.*639C>G	ENSP00000497513.1:n.*639C>G
ENST00000649606.1:n.676C>G
ENST00000649895.1:n.881C>G
ENST00000650197.1:c.663C>G	ENSP00000496929.1:p.Thr221=
ENST00000367435.3:c.663C>G	ENSP00000356405.3:p.Thr221=
NM_024529.4:c.663C>G , LRG_507t1:c.663C>G	NP_078805.3:p.Thr221=
XM_006711537.2:c.663C>G	XP_006711600.1:p.Thr221=
XM_006711537.4:c.663C>G	XP_006711600.1:p.Thr221=
NM_024529.5:c.663C>G MANE Select	NP_078805.3:p.Thr221=