Canonical Allele Identifier: CA136036851
Gene: RNF39 HGNC NCBI

Linked Data

dbSNP Id: rs964600419

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30072992_30072995del , CM000668.2:g.30072992_30072995del GRCh38
NC_000006.11:g.30040769_30040772del , CM000668.1:g.30040769_30040772del GRCh37
NC_000006.10:g.30148748_30148751del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000244360.8:c.478+164_478+167del MANE Select ENSP00000244360.7:n.478+164_478+167del
ENST00000244360.7:c.478+164_478+167del ENSP00000244360.7:n.478+164_478+167del
ENST00000376751.8:c.478+164_478+167del ENSP00000365942.4:n.478+164_478+167del
ENST00000244360.6:c.682+164_682+167del ENSP00000244360.6:n.682+164_682+167del
ENST00000376751.7:c.682+164_682+167del ENSP00000365942.3:n.682+164_682+167del
NM_025236.3:c.682+164_682+167del NP_079512.2:n.682+164_682+167del
NM_170769.2:c.682+164_682+167del NP_739575.2:n.682+164_682+167del
XM_017011325.1:c.223+164_223+167del XP_016866814.1:n.223+164_223+167del
XM_017011326.1:c.682+164_682+167del XP_016866815.1:n.682+164_682+167del
NM_025236.4:c.478+164_478+167del MANE Select NP_079512.3:n.478+164_478+167del
NM_170769.3:c.478+164_478+167del NP_739575.3:n.478+164_478+167del