Canonical Allele Identifier: CA1148224804

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122332G= , CM000663.2:g.193122332G=	GRCh38
NC_000001.10:g.193091462G= , CM000663.1:g.193091462G=	GRCh37
NC_000001.9:g.191358085G=	NCBI36
NG_012691.1:g.5375G= , LRG_507:g.5375G=

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.131+1G= MANE Select	NP_078805.3:n.131+1G=
ENST00000367435.5:c.131+1G= MANE Select	ENSP00000356405.4:n.131+1G=
NM_024529.4:c.131+1G= , LRG_507t1:c.131+1G=	NP_078805.3:n.131+1G=
ENST00000367435.3:c.131+1G=	ENSP00000356405.3:n.131+1G=
ENST00000635846.1:c.131+1G=	ENSP00000490035.1:n.131+1G=
ENST00000643006.1:c.131+1G=	ENSP00000496633.1:n.131+1G=
ENST00000643784.1:c.131+1G=	ENSP00000494944.1:n.131+1G=
ENST00000647662.1:n.32+1G=
ENST00000648071.1:c.131+1G=	ENSP00000497513.1:n.131+1G=
ENST00000649606.1:n.144+1G=
ENST00000649895.1:n.349+1G=
ENST00000650197.1:c.131+1G=	ENSP00000496929.1:n.131+1G=
XM_006711537.2:c.131+1G=	XP_006711600.1:n.131+1G=
XM_006711537.4:c.131+1G=	XP_006711600.1:n.131+1G=
XR_001738350.1:n.1325C=