Canonical Allele Identifier: CA729323025

Gene: CDC73

Linked Data

• dbSNP Id: rs1318830558
• MyVariant Identifiers: chr1:g.193220740C>A (hg19) ; chr1:g.193251610C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251610C>A , CM000663.2:g.193251610C>A	GRCh38
NC_000001.10:g.193220740C>A , CM000663.1:g.193220740C>A	GRCh37
NC_000001.9:g.191487363C>A	NCBI36
NG_012691.1:g.134653C>A , LRG_507:g.134653C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*898C>A MANE Select	ENSP00000356405.4:n.*898C>A
ENST00000635846.1:c.*898C>A	ENSP00000490035.1:n.*898C>A
ENST00000643006.1:c.*1404C>A	ENSP00000496633.1:n.*1404C>A
ENST00000367435.3:c.*898C>A	ENSP00000356405.3:n.*898C>A
NM_024529.4:c.*898C>A , LRG_507t1:c.*898C>A	NP_078805.3:n.*898C>A
NM_024529.5:c.*898C>A MANE Select	NP_078805.3:n.*898C>A