Canonical Allele Identifier: CA1618577309
Gene: RNF39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30072945A= , CM000668.2:g.30072945A= GRCh38
NC_000006.11:g.30040722A= , CM000668.1:g.30040722A= GRCh37
NC_000006.10:g.30148701A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000244360.8:c.478+212T= MANE Select ENSP00000244360.7:n.478+212T=
ENST00000244360.7:c.478+212T= ENSP00000244360.7:n.478+212T=
ENST00000376751.8:c.478+212T= ENSP00000365942.4:n.478+212T=
ENST00000244360.6:c.682+212T= ENSP00000244360.6:n.682+212T=
ENST00000376751.7:c.682+212T= ENSP00000365942.3:n.682+212T=
NM_025236.3:c.682+212T= NP_079512.2:n.682+212T=
NM_170769.2:c.682+212T= NP_739575.2:n.682+212T=
XM_017011325.1:c.223+212T= XP_016866814.1:n.223+212T=
XM_017011326.1:c.682+212T= XP_016866815.1:n.682+212T=
NM_025236.4:c.478+212T= MANE Select NP_079512.3:n.478+212T=
NM_170769.3:c.478+212T= NP_739575.3:n.478+212T=
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