Canonical Allele Identifier: CA422348682

Gene: CDC73

Linked Data

• dbSNP Id: rs2103111637
• MyVariant Identifiers: chr1:g.193091369C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122239C>A , CM000663.2:g.193122239C>A	GRCh38
NC_000001.10:g.193091369C>A , CM000663.1:g.193091369C>A	GRCh37
NC_000001.9:g.191357992C>A	NCBI36
NG_012691.1:g.5282C>A , LRG_507:g.5282C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.39C>A MANE Select	ENSP00000356405.4:p.Ile13=
ENST00000635846.1:c.39C>A	ENSP00000490035.1:p.Ile13=
ENST00000643006.1:c.39C>A	ENSP00000496633.1:p.Ile13=
ENST00000643784.1:c.39C>A	ENSP00000494944.1:p.Ile13=
ENST00000648071.1:c.39C>A	ENSP00000497513.1:p.Ile13=
ENST00000649606.1:n.52C>A
ENST00000649895.1:n.257C>A
ENST00000650197.1:c.39C>A	ENSP00000496929.1:p.Ile13=
ENST00000367435.3:c.39C>A	ENSP00000356405.3:p.Ile13=
NM_024529.4:c.39C>A , LRG_507t1:c.39C>A	NP_078805.3:p.Ile13=
XM_006711537.2:c.39C>A	XP_006711600.1:p.Ile13=
XM_006711537.4:c.39C>A	XP_006711600.1:p.Ile13=
XR_001738350.1:n.1418G>T
NM_024529.5:c.39C>A MANE Select	NP_078805.3:p.Ile13=