Canonical Allele Identifier: CA344076097

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193172934T>A (hg19) ; chr1:g.193203804T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203804T>A , CM000663.2:g.193203804T>A	GRCh38
NC_000001.10:g.193172934T>A , CM000663.1:g.193172934T>A	GRCh37
NC_000001.9:g.191439557T>A	NCBI36
NG_012691.1:g.86847T>A , LRG_507:g.86847T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.982T>A MANE Select	ENSP00000356405.4:p.Ser328Thr
ENST00000635846.1:c.739T>A	ENSP00000490035.1:p.Ser247Thr
ENST00000643006.1:c.1050T>A	ENSP00000496633.1:p.His350Gln
ENST00000648071.1:c.*958T>A	ENSP00000497513.1:n.*958T>A
ENST00000649613.1:n.232T>A
ENST00000649895.1:n.1200T>A
ENST00000650197.1:c.982T>A	ENSP00000496929.1:p.Ser328Thr
ENST00000367435.3:c.982T>A	ENSP00000356405.3:p.Ser328Thr
NM_024529.4:c.982T>A , LRG_507t1:c.982T>A	NP_078805.3:p.Ser328Thr
NM_024529.5:c.982T>A MANE Select	NP_078805.3:p.Ser328Thr