Canonical Allele Identifier: CA1303395

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193138111A>G , CM000663.2:g.193138111A>G	GRCh38
NC_000001.10:g.193107241A>G , CM000663.1:g.193107241A>G	GRCh37
NC_000001.9:g.191373864A>G	NCBI36
NG_012691.1:g.21154A>G , LRG_507:g.21154A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.450A>G MANE Select	NP_078805.3:p.Lys150=
ENST00000367435.5:c.450A>G MANE Select	ENSP00000356405.4:p.Lys150=
NM_024529.4:c.450A>G , LRG_507t1:c.450A>G	NP_078805.3:p.Lys150=
ENST00000367435.3:c.450A>G	ENSP00000356405.3:p.Lys150=
ENST00000482484.1:n.702A>G
ENST00000635846.1:c.450A>G	ENSP00000490035.1:p.Lys150=
ENST00000643006.1:c.450A>G	ENSP00000496633.1:p.Lys150=
ENST00000643784.1:c.450A>G	ENSP00000494944.1:p.Lys150=
ENST00000647662.1:n.351A>G
ENST00000648071.1:c.*426A>G	ENSP00000497513.1:n.*426A>G
ENST00000649606.1:n.463A>G
ENST00000649706.1:n.391A>G
ENST00000649895.1:n.668A>G
ENST00000650197.1:c.450A>G	ENSP00000496929.1:p.Lys150=
XM_006711537.2:c.450A>G	XP_006711600.1:p.Lys150=
XM_006711537.4:c.450A>G	XP_006711600.1:p.Lys150=