Canonical Allele Identifier: CA2649631035
Gene: CDC73 HGNC NCBI

Linked Data

gnomAD v4: 1-193251517-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251521del , CM000663.2:g.193251521del GRCh38
NC_000001.10:g.193220651del , CM000663.1:g.193220651del GRCh37
NC_000001.9:g.191487274del NCBI36
NG_012691.1:g.134564del , LRG_507:g.134564del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*809del MANE Select ENSP00000356405.4:n.*809del
ENST00000635846.1:c.*809del ENSP00000490035.1:n.*809del
ENST00000643006.1:c.*1315del ENSP00000496633.1:n.*1315del
ENST00000367435.3:c.*809del ENSP00000356405.3:n.*809del
NM_024529.4:c.*809del , LRG_507t1:c.*809del NP_078805.3:n.*809del
NM_024529.5:c.*809del MANE Select NP_078805.3:n.*809del
Search 100 bp 5'
Search 100 bp 3'