Canonical Allele Identifier: CA1216149952

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203752A= , CM000663.2:g.193203752A=	GRCh38
NC_000001.10:g.193172882A= , CM000663.1:g.193172882A=	GRCh37
NC_000001.9:g.191439505A=	NCBI36
NG_012691.1:g.86795A= , LRG_507:g.86795A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-43A= MANE Select	ENSP00000356405.4:n.973-43A=
ENST00000635846.1:c.730-43A=	ENSP00000490035.1:n.730-43A=
ENST00000643006.1:c.1041-43A=	ENSP00000496633.1:n.1041-43A=
ENST00000648071.1:c.*949-43A=	ENSP00000497513.1:n.*949-43A=
ENST00000649613.1:n.223-43A=
ENST00000649895.1:n.1191-43A=
ENST00000650197.1:c.973-43A=	ENSP00000496929.1:n.973-43A=
ENST00000367435.3:c.973-43A=	ENSP00000356405.3:n.973-43A=
NM_024529.4:c.973-43A= , LRG_507t1:c.973-43A=	NP_078805.3:n.973-43A=
NM_024529.5:c.973-43A= MANE Select	NP_078805.3:n.973-43A=