Canonical Allele Identifier: CA1216122079

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193141950A= , CM000663.2:g.193141950A=	GRCh38
NC_000001.10:g.193111080A= , CM000663.1:g.193111080A=	GRCh37
NC_000001.9:g.191377703A=	NCBI36
NG_012691.1:g.24993A= , LRG_507:g.24993A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.613A= MANE Select	ENSP00000356405.4:p.Ile205=
ENST00000635846.1:c.613A=	ENSP00000490035.1:p.Ile205=
ENST00000643006.1:c.613A=	ENSP00000496633.1:p.Ile205=
ENST00000643784.1:c.*89A=	ENSP00000494944.1:n.*89A=
ENST00000647662.1:n.514A=
ENST00000648071.1:c.*589A=	ENSP00000497513.1:n.*589A=
ENST00000649606.1:n.626A=
ENST00000649706.1:n.554A=
ENST00000649895.1:n.831A=
ENST00000650197.1:c.613A=	ENSP00000496929.1:p.Ile205=
ENST00000367435.3:c.613A=	ENSP00000356405.3:p.Ile205=
NM_024529.4:c.613A= , LRG_507t1:c.613A=	NP_078805.3:p.Ile205=
XM_006711537.2:c.613A=	XP_006711600.1:p.Ile205=
XM_006711537.4:c.613A=	XP_006711600.1:p.Ile205=
NM_024529.5:c.613A= MANE Select	NP_078805.3:p.Ile205=