Canonical Allele Identifier: CA549097985
Gene: ZNF732 HGNC NCBI

Linked Data

dbSNP Id: rs1553840944
gnomAD v2: 4-282410-ACT-A
MyVariant Identifiers: chr4:g.282411_282412del (hg19) chr4:g.288622_288623del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.288622_288623del , CM000666.2:g.288622_288623del GRCh38
NC_000004.11:g.282411_282412del , CM000666.1:g.282411_282412del GRCh37
NC_000004.10:g.272411_272412del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419098.6:c.226+6815_226+6816del MANE Select ENSP00000415774.1:n.226+6815_226+6816del
ENST00000419098.5:c.226+6815_226+6816del ENSP00000415774.1:n.226+6815_226+6816del
ENST00000619749.1:c.223+6815_223+6816del ENSP00000478210.1:n.223+6815_223+6816del
NM_001137608.1:c.226+6815_226+6816del NP_001131080.1:n.226+6815_226+6816del
NM_001137608.2:c.226+6815_226+6816del NP_001131080.1:n.226+6815_226+6816del
NM_001137608.3:c.226+6815_226+6816del MANE Select NP_001131080.1:n.226+6815_226+6816del
Search 100 bp 5'
Search 100 bp 3'