Canonical Allele Identifier: CA422349973

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193125118A>T , CM000663.2:g.193125118A>T	GRCh38
NC_000001.10:g.193094248A>T , CM000663.1:g.193094248A>T	GRCh37
NC_000001.9:g.191360871A>T	NCBI36
NG_012691.1:g.8161A>T , LRG_507:g.8161A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.138A>T MANE Select	NP_078805.3:p.Gly46=
ENST00000367435.5:c.138A>T MANE Select	ENSP00000356405.4:p.Gly46=
NM_024529.4:c.138A>T , LRG_507t1:c.138A>T	NP_078805.3:p.Gly46=
ENST00000367435.3:c.138A>T	ENSP00000356405.3:p.Gly46=
ENST00000482484.1:n.99A>T
ENST00000635846.1:c.138A>T	ENSP00000490035.1:p.Gly46=
ENST00000643006.1:c.138A>T	ENSP00000496633.1:p.Gly46=
ENST00000643784.1:c.138A>T	ENSP00000494944.1:p.Gly46=
ENST00000647662.1:n.39A>T
ENST00000648071.1:c.138A>T	ENSP00000497513.1:p.Gly46=
ENST00000649606.1:n.151A>T
ENST00000649706.1:n.79A>T
ENST00000649895.1:n.356A>T
ENST00000650197.1:c.138A>T	ENSP00000496929.1:p.Gly46=
XM_006711537.2:c.138A>T	XP_006711600.1:p.Gly46=
XM_006711537.4:c.138A>T	XP_006711600.1:p.Gly46=
XR_241165.2:n.304-811T>A