Canonical Allele Identifier: CA34379488

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193150351A>G , CM000663.2:g.193150351A>G	GRCh38
NC_000001.10:g.193119481A>G , CM000663.1:g.193119481A>G	GRCh37
NC_000001.9:g.191386104A>G	NCBI36
NG_012691.1:g.33394A>G , LRG_507:g.33394A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.876A>G MANE Select	NP_078805.3:p.Arg292=
ENST00000367435.5:c.876A>G MANE Select	ENSP00000356405.4:p.Arg292=
NM_024529.4:c.876A>G , LRG_507t1:c.876A>G	NP_078805.3:p.Arg292=
ENST00000367435.3:c.876A>G	ENSP00000356405.3:p.Arg292=
ENST00000635846.1:c.729+8285A>G	ENSP00000490035.1:n.729+8285A>G
ENST00000643006.1:c.876A>G	ENSP00000496633.1:p.Arg292=
ENST00000643784.1:c.*352A>G	ENSP00000494944.1:n.*352A>G
ENST00000647662.1:n.777A>G
ENST00000648071.1:c.*852A>G	ENSP00000497513.1:n.*852A>G
ENST00000649606.1:n.889A>G
ENST00000649895.1:n.1094A>G
ENST00000650197.1:c.876A>G	ENSP00000496929.1:p.Arg292=
XM_006711537.2:c.876A>G	XP_006711600.1:p.Arg292=
XM_006711537.4:c.876A>G	XP_006711600.1:p.Arg292=