Canonical Allele Identifier: CA729322949

Gene: CDC73

Linked Data

• dbSNP Id: rs1235444911
• MyVariant Identifiers: chr1:g.193220570A>T (hg19) ; chr1:g.193251440A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251440A>T , CM000663.2:g.193251440A>T	GRCh38
NC_000001.10:g.193220570A>T , CM000663.1:g.193220570A>T	GRCh37
NC_000001.9:g.191487193A>T	NCBI36
NG_012691.1:g.134483A>T , LRG_507:g.134483A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*728A>T MANE Select	ENSP00000356405.4:n.*728A>T
ENST00000635846.1:c.*728A>T	ENSP00000490035.1:n.*728A>T
ENST00000643006.1:c.*1234A>T	ENSP00000496633.1:n.*1234A>T
ENST00000367435.3:c.*728A>T	ENSP00000356405.3:n.*728A>T
NM_024529.4:c.*728A>T , LRG_507t1:c.*728A>T	NP_078805.3:n.*728A>T
NM_024529.5:c.*728A>T MANE Select	NP_078805.3:n.*728A>T