Canonical Allele Identifier: CA344078428

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193218902C>G (hg19) ; chr1:g.193249772C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193249772C>G , CM000663.2:g.193249772C>G	GRCh38
NC_000001.10:g.193218902C>G , CM000663.1:g.193218902C>G	GRCh37
NC_000001.9:g.191485525C>G	NCBI36
NG_012691.1:g.132815C>G , LRG_507:g.132815C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1460C>G MANE Select	ENSP00000356405.4:p.Pro487Arg
ENST00000635846.1:c.1217C>G	ENSP00000490035.1:p.Pro406Arg
ENST00000643006.1:c.*370C>G	ENSP00000496633.1:n.*370C>G
ENST00000648071.1:c.*1436C>G	ENSP00000497513.1:n.*1436C>G
ENST00000649613.1:n.710C>G
ENST00000650197.1:c.*158C>G	ENSP00000496929.1:n.*158C>G
ENST00000367435.3:c.1460C>G	ENSP00000356405.3:p.Pro487Arg
ENST00000477868.1:n.172C>G
NM_024529.4:c.1460C>G , LRG_507t1:c.1460C>G	NP_078805.3:p.Pro487Arg
NM_024529.5:c.1460C>G MANE Select	NP_078805.3:p.Pro487Arg