Canonical Allele Identifier: CA2580061780
Community Standard Title: NM_024529.5(CDC73):c.1317-3T>C
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193236253T>C , CM000663.2:g.193236253T>C GRCh38
NC_000001.10:g.193205383T>C , CM000663.1:g.193205383T>C GRCh37
NC_000001.9:g.191472006T>C NCBI36
NG_012691.1:g.119296T>C , LRG_507:g.119296T>C

Transcript Alleles

HGVS Amino-acid Change
NM_024529.5:c.1317-3T>C MANE Select NP_078805.3:n.1317-3T>C
ENST00000367435.5:c.1317-3T>C MANE Select ENSP00000356405.4:n.1317-3T>C
NM_024529.4:c.1317-3T>C , LRG_507t1:c.1317-3T>C NP_078805.3:n.1317-3T>C
ENST00000367435.3:c.1317-3T>C ENSP00000356405.3:n.1317-3T>C
ENST00000477868.1:n.129+3099T>C
ENST00000635846.1:c.1074-3T>C ENSP00000490035.1:n.1074-3T>C
ENST00000643006.1:c.*227-3T>C ENSP00000496633.1:n.*227-3T>C
ENST00000648071.1:c.*1293-3T>C ENSP00000497513.1:n.*1293-3T>C
ENST00000649613.1:n.567-3T>C
ENST00000649895.1:n.1535-3T>C
ENST00000650197.1:c.1317-3T>C ENSP00000496929.1:n.1317-3T>C