Canonical Allele Identifier: CA1303418

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193141842G>T , CM000663.2:g.193141842G>T	GRCh38
NC_000001.10:g.193110972G>T , CM000663.1:g.193110972G>T	GRCh37
NC_000001.9:g.191377595G>T	NCBI36
NG_012691.1:g.24885G>T , LRG_507:g.24885G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.513-8G>T MANE Select	NP_078805.3:n.513-8G>T
ENST00000367435.5:c.513-8G>T MANE Select	ENSP00000356405.4:n.513-8G>T
NM_024529.4:c.513-8G>T , LRG_507t1:c.513-8G>T	NP_078805.3:n.513-8G>T
ENST00000367435.3:c.513-8G>T	ENSP00000356405.3:n.513-8G>T
ENST00000635846.1:c.513-8G>T	ENSP00000490035.1:n.513-8G>T
ENST00000643006.1:c.513-8G>T	ENSP00000496633.1:n.513-8G>T
ENST00000643784.1:c.583-8G>T	ENSP00000494944.1:n.583-8G>T
ENST00000647662.1:n.414-8G>T
ENST00000648071.1:c.*489-8G>T	ENSP00000497513.1:n.*489-8G>T
ENST00000649606.1:n.526-8G>T
ENST00000649706.1:n.454-8G>T
ENST00000649895.1:n.731-8G>T
ENST00000650197.1:c.513-8G>T	ENSP00000496929.1:n.513-8G>T
XM_006711537.2:c.513-8G>T	XP_006711600.1:n.513-8G>T
XM_006711537.4:c.513-8G>T	XP_006711600.1:n.513-8G>T