Canonical Allele Identifier: CA343962773

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193111158T>G (hg19) ; chr1:g.193142028T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142028T>G , CM000663.2:g.193142028T>G	GRCh38
NC_000001.10:g.193111158T>G , CM000663.1:g.193111158T>G	GRCh37
NC_000001.9:g.191377781T>G	NCBI36
NG_012691.1:g.25071T>G , LRG_507:g.25071T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.691T>G MANE Select	ENSP00000356405.4:p.Trp231Gly
ENST00000635846.1:c.691T>G	ENSP00000490035.1:p.Trp231Gly
ENST00000643006.1:c.691T>G	ENSP00000496633.1:p.Trp231Gly
ENST00000643784.1:c.*167T>G	ENSP00000494944.1:n.*167T>G
ENST00000647662.1:n.592T>G
ENST00000648071.1:c.*667T>G	ENSP00000497513.1:n.*667T>G
ENST00000649606.1:n.704T>G
ENST00000649895.1:n.909T>G
ENST00000650197.1:c.691T>G	ENSP00000496929.1:p.Trp231Gly
ENST00000367435.3:c.691T>G	ENSP00000356405.3:p.Trp231Gly
NM_024529.4:c.691T>G , LRG_507t1:c.691T>G	NP_078805.3:p.Trp231Gly
XM_006711537.2:c.691T>G	XP_006711600.1:p.Trp231Gly
XM_006711537.4:c.691T>G	XP_006711600.1:p.Trp231Gly
NM_024529.5:c.691T>G MANE Select	NP_078805.3:p.Trp231Gly