Canonical Allele Identifier: CA1216122144

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142116A= , CM000663.2:g.193142116A=	GRCh38
NC_000001.10:g.193111246A= , CM000663.1:g.193111246A=	GRCh37
NC_000001.9:g.191377869A=	NCBI36
NG_012691.1:g.25159A= , LRG_507:g.25159A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.729+50A= MANE Select	ENSP00000356405.4:n.729+50A=
ENST00000635846.1:c.729+50A=	ENSP00000490035.1:n.729+50A=
ENST00000643006.1:c.729+50A=	ENSP00000496633.1:n.729+50A=
ENST00000643784.1:c.*205+50A=	ENSP00000494944.1:n.*205+50A=
ENST00000647662.1:n.630+50A=
ENST00000648071.1:c.*705+50A=	ENSP00000497513.1:n.*705+50A=
ENST00000649606.1:n.742+50A=
ENST00000649895.1:n.947+50A=
ENST00000650197.1:c.729+50A=	ENSP00000496929.1:n.729+50A=
ENST00000367435.3:c.729+50A=	ENSP00000356405.3:n.729+50A=
NM_024529.4:c.729+50A= , LRG_507t1:c.729+50A=	NP_078805.3:n.729+50A=
XM_006711537.2:c.729+50A=	XP_006711600.1:n.729+50A=
XM_006711537.4:c.729+50A=	XP_006711600.1:n.729+50A=
NM_024529.5:c.729+50A= MANE Select	NP_078805.3:n.729+50A=