Canonical Allele Identifier: CA2747148451
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251881_193251882insTTTTTT , CM000663.2:g.193251881_193251882insTTTTTT GRCh38
NC_000001.10:g.193221011_193221012insTTTTTT , CM000663.1:g.193221011_193221012insTTTTTT GRCh37
NC_000001.9:g.191487634_191487635insTTTTTT NCBI36
NG_012691.1:g.134924_134925insTTTTTT , LRG_507:g.134924_134925insTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1169_*1170insTTTTTT MANE Select ENSP00000356405.4:n.*1169_*1170insTTTTTT
ENST00000635846.1:c.*1169_*1170insTTTTTT ENSP00000490035.1:n.*1169_*1170insTTTTTT
ENST00000643006.1:c.*1675_*1676insTTTTTT ENSP00000496633.1:n.*1675_*1676insTTTTTT
ENST00000367435.3:c.*1169_*1170insTTTTTT ENSP00000356405.3:n.*1169_*1170insTTTTTT
NM_024529.4:c.*1169_*1170insTTTTTT , LRG_507t1:c.*1169_*1170insTTTTTT NP_078805.3:n.*1169_*1170insTTTTTT
NM_024529.5:c.*1169_*1170insTTTTTT MANE Select NP_078805.3:n.*1169_*1170insTTTTTT