Canonical Allele Identifier: CA1216149942

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203713T= , CM000663.2:g.193203713T=	GRCh38
NC_000001.10:g.193172843T= , CM000663.1:g.193172843T=	GRCh37
NC_000001.9:g.191439466T=	NCBI36
NG_012691.1:g.86756T= , LRG_507:g.86756T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-82T= MANE Select	ENSP00000356405.4:n.973-82T=
ENST00000635846.1:c.730-82T=	ENSP00000490035.1:n.730-82T=
ENST00000643006.1:c.1041-82T=	ENSP00000496633.1:n.1041-82T=
ENST00000648071.1:c.*949-82T=	ENSP00000497513.1:n.*949-82T=
ENST00000649613.1:n.223-82T=
ENST00000649895.1:n.1191-82T=
ENST00000650197.1:c.973-82T=	ENSP00000496929.1:n.973-82T=
ENST00000367435.3:c.973-82T=	ENSP00000356405.3:n.973-82T=
NM_024529.4:c.973-82T= , LRG_507t1:c.973-82T=	NP_078805.3:n.973-82T=
NM_024529.5:c.973-82T= MANE Select	NP_078805.3:n.973-82T=