Canonical Allele Identifier: CA1216149944

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203715T= , CM000663.2:g.193203715T=	GRCh38
NC_000001.10:g.193172845T= , CM000663.1:g.193172845T=	GRCh37
NC_000001.9:g.191439468T=	NCBI36
NG_012691.1:g.86758T= , LRG_507:g.86758T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-80T= MANE Select	ENSP00000356405.4:n.973-80T=
ENST00000635846.1:c.730-80T=	ENSP00000490035.1:n.730-80T=
ENST00000643006.1:c.1041-80T=	ENSP00000496633.1:n.1041-80T=
ENST00000648071.1:c.*949-80T=	ENSP00000497513.1:n.*949-80T=
ENST00000649613.1:n.223-80T=
ENST00000649895.1:n.1191-80T=
ENST00000650197.1:c.973-80T=	ENSP00000496929.1:n.973-80T=
ENST00000367435.3:c.973-80T=	ENSP00000356405.3:n.973-80T=
NM_024529.4:c.973-80T= , LRG_507t1:c.973-80T=	NP_078805.3:n.973-80T=
NM_024529.5:c.973-80T= MANE Select	NP_078805.3:n.973-80T=