Canonical Allele Identifier: CA1216149940

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203707G= , CM000663.2:g.193203707G=	GRCh38
NC_000001.10:g.193172837G= , CM000663.1:g.193172837G=	GRCh37
NC_000001.9:g.191439460G=	NCBI36
NG_012691.1:g.86750G= , LRG_507:g.86750G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-88G= MANE Select	ENSP00000356405.4:n.973-88G=
ENST00000635846.1:c.730-88G=	ENSP00000490035.1:n.730-88G=
ENST00000643006.1:c.1041-88G=	ENSP00000496633.1:n.1041-88G=
ENST00000648071.1:c.*949-88G=	ENSP00000497513.1:n.*949-88G=
ENST00000649613.1:n.223-88G=
ENST00000649895.1:n.1191-88G=
ENST00000650197.1:c.973-88G=	ENSP00000496929.1:n.973-88G=
ENST00000367435.3:c.973-88G=	ENSP00000356405.3:n.973-88G=
NM_024529.4:c.973-88G= , LRG_507t1:c.973-88G=	NP_078805.3:n.973-88G=
NM_024529.5:c.973-88G= MANE Select	NP_078805.3:n.973-88G=