Canonical Allele Identifier: CA422345178

Gene: CDC73

Linked Data

• dbSNP Id: rs1376027438
• MyVariant Identifiers: chr1:g.193111133A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142003A>T , CM000663.2:g.193142003A>T	GRCh38
NC_000001.10:g.193111133A>T , CM000663.1:g.193111133A>T	GRCh37
NC_000001.9:g.191377756A>T	NCBI36
NG_012691.1:g.25046A>T , LRG_507:g.25046A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.666A>T MANE Select	ENSP00000356405.4:p.Arg222=
ENST00000635846.1:c.666A>T	ENSP00000490035.1:p.Arg222=
ENST00000643006.1:c.666A>T	ENSP00000496633.1:p.Arg222=
ENST00000643784.1:c.*142A>T	ENSP00000494944.1:n.*142A>T
ENST00000647662.1:n.567A>T
ENST00000648071.1:c.*642A>T	ENSP00000497513.1:n.*642A>T
ENST00000649606.1:n.679A>T
ENST00000649895.1:n.884A>T
ENST00000650197.1:c.666A>T	ENSP00000496929.1:p.Arg222=
ENST00000367435.3:c.666A>T	ENSP00000356405.3:p.Arg222=
NM_024529.4:c.666A>T , LRG_507t1:c.666A>T	NP_078805.3:p.Arg222=
XM_006711537.2:c.666A>T	XP_006711600.1:p.Arg222=
XM_006711537.4:c.666A>T	XP_006711600.1:p.Arg222=
NM_024529.5:c.666A>T MANE Select	NP_078805.3:p.Arg222=