Canonical Allele Identifier: CA343962847

Gene: CDC73

Linked Data

• gnomAD v4: 1-193142061-G-A
• MyVariant Identifiers: chr1:g.193111191G>A (hg19) ; chr1:g.193142061G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142061G>A , CM000663.2:g.193142061G>A	GRCh38
NC_000001.10:g.193111191G>A , CM000663.1:g.193111191G>A	GRCh37
NC_000001.9:g.191377814G>A	NCBI36
NG_012691.1:g.25104G>A , LRG_507:g.25104G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.724G>A MANE Select	ENSP00000356405.4:p.Gly242Arg
ENST00000635846.1:c.724G>A	ENSP00000490035.1:p.Gly242Arg
ENST00000643006.1:c.724G>A	ENSP00000496633.1:p.Gly242Arg
ENST00000643784.1:c.*200G>A	ENSP00000494944.1:n.*200G>A
ENST00000647662.1:n.625G>A
ENST00000648071.1:c.*700G>A	ENSP00000497513.1:n.*700G>A
ENST00000649606.1:n.737G>A
ENST00000649895.1:n.942G>A
ENST00000650197.1:c.724G>A	ENSP00000496929.1:p.Gly242Arg
ENST00000367435.3:c.724G>A	ENSP00000356405.3:p.Gly242Arg
NM_024529.4:c.724G>A , LRG_507t1:c.724G>A	NP_078805.3:p.Gly242Arg
XM_006711537.2:c.724G>A	XP_006711600.1:p.Gly242Arg
XM_006711537.4:c.724G>A	XP_006711600.1:p.Gly242Arg
NM_024529.5:c.724G>A MANE Select	NP_078805.3:p.Gly242Arg