Canonical Allele Identifier: CA2368297124
Gene: RNF114 HGNC NCBI

Linked Data

dbSNP Id: rs2235617
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49938440C>A , CM000682.2:g.49938440C>A GRCh38
NC_000020.10:g.48554977C>A , CM000682.1:g.48554977C>A GRCh37
NC_000020.9:g.47988384C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244061.6:c.140+1888C>A MANE Select ENSP00000244061.2:n.140+1888C>A
ENST00000244061.5:c.140+1888C>A ENSP00000244061.2:n.140+1888C>A
ENST00000622920.1:c.140+1888C>A ENSP00000485317.1:n.140+1888C>A
ENST00000622999.3:c.140+1888C>A ENSP00000485203.1:n.140+1888C>A
ENST00000623528.3:c.140+1888C>A ENSP00000485136.1:n.140+1888C>A
ENST00000623732.3:c.140+1888C>A ENSP00000485575.1:n.140+1888C>A
ENST00000624620.1:n.154+1888C>A
ENST00000625177.3:c.140+1888C>A ENSP00000485239.1:n.140+1888C>A
NM_018683.3:c.140+1888C>A NP_061153.1:n.140+1888C>A
NM_018683.4:c.140+1888C>A MANE Select NP_061153.1:n.140+1888C>A
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