Canonical Allele Identifier: CA1432667957
Gene: ZNF732 HGNC NCBI

Linked Data

dbSNP Id: rs1719779503
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.288627_288635del , CM000666.2:g.288627_288635del GRCh38
NC_000004.11:g.282416_282424del , CM000666.1:g.282416_282424del GRCh37
NC_000004.10:g.272416_272424del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419098.6:c.226+6804_226+6812del MANE Select ENSP00000415774.1:n.226+6804_226+6812del
ENST00000419098.5:c.226+6804_226+6812del ENSP00000415774.1:n.226+6804_226+6812del
ENST00000619749.1:c.223+6804_223+6812del ENSP00000478210.1:n.223+6804_223+6812del
NM_001137608.1:c.226+6804_226+6812del NP_001131080.1:n.226+6804_226+6812del
NM_001137608.2:c.226+6804_226+6812del NP_001131080.1:n.226+6804_226+6812del
NM_001137608.3:c.226+6804_226+6812del MANE Select NP_001131080.1:n.226+6804_226+6812del
Search 100 bp 5'
Search 100 bp 3'