Canonical Allele Identifier: CA1216170283

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193249727T>C , CM000663.2:g.193249727T>C	GRCh38
NC_000001.10:g.193218857T>C , CM000663.1:g.193218857T>C	GRCh37
NC_000001.9:g.191485480T>C	NCBI36
NG_012691.1:g.132770T>C , LRG_507:g.132770T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.1418-3T>C MANE Select	NP_078805.3:n.1418-3T>C
ENST00000367435.5:c.1418-3T>C MANE Select	ENSP00000356405.4:n.1418-3T>C
NM_024529.4:c.1418-3T>C , LRG_507t1:c.1418-3T>C	NP_078805.3:n.1418-3T>C
ENST00000367435.3:c.1418-3T>C	ENSP00000356405.3:n.1418-3T>C
ENST00000477868.1:n.130-3T>C
ENST00000635846.1:c.1175-3T>C	ENSP00000490035.1:n.1175-3T>C
ENST00000643006.1:c.*328-3T>C	ENSP00000496633.1:n.*328-3T>C
ENST00000648071.1:c.*1394-3T>C	ENSP00000497513.1:n.*1394-3T>C
ENST00000649613.1:n.668-3T>C
ENST00000650197.1:c.*116-3T>C	ENSP00000496929.1:n.*116-3T>C