Canonical Allele Identifier: CA916081296

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193249875A>T , CM000663.2:g.193249875A>T	GRCh38
NC_000001.10:g.193219005A>T , CM000663.1:g.193219005A>T	GRCh37
NC_000001.9:g.191485628A>T	NCBI36
NG_012691.1:g.132918A>T , LRG_507:g.132918A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.1559+4A>T MANE Select	NP_078805.3:n.1559+4A>T
ENST00000367435.5:c.1559+4A>T MANE Select	ENSP00000356405.4:n.1559+4A>T
NM_024529.4:c.1559+4A>T , LRG_507t1:c.1559+4A>T	NP_078805.3:n.1559+4A>T
ENST00000367435.3:c.1559+4A>T	ENSP00000356405.3:n.1559+4A>T
ENST00000477868.1:n.271+4A>T
ENST00000635846.1:c.1316+4A>T	ENSP00000490035.1:n.1316+4A>T
ENST00000643006.1:c.*469+4A>T	ENSP00000496633.1:n.*469+4A>T
ENST00000648071.1:c.*1535+4A>T	ENSP00000497513.1:n.*1535+4A>T
ENST00000649613.1:n.809+4A>T
ENST00000650197.1:c.*257+4A>T	ENSP00000496929.1:n.*257+4A>T