Canonical Allele Identifier: CA1618577419

Gene: RNF39

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30073232A= , CM000668.2:g.30073232A=	GRCh38
NC_000006.11:g.30041009A= , CM000668.1:g.30041009A=	GRCh37
NC_000006.10:g.30148988A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025236.4:c.403T= MANE Select	NP_079512.3:p.Ser135=
ENST00000244360.8:c.403T= MANE Select	ENSP00000244360.7:p.Ser135=
NM_025236.3:c.607T=	NP_079512.2:p.Ser203=
NM_170769.2:c.607T=	NP_739575.2:p.Ser203=
NM_170769.3:c.403T=	NP_739575.3:p.Ser135=
ENST00000244360.6:c.607T=	ENSP00000244360.6:p.Ser203=
ENST00000244360.7:c.403T=	ENSP00000244360.7:p.Ser135=
ENST00000376751.7:c.607T=	ENSP00000365942.3:p.Ser203=
ENST00000376751.8:c.403T=	ENSP00000365942.4:p.Ser135=
XM_017011325.1:c.148T=	XP_016866814.1:p.Ser50=
XM_017011326.1:c.607T=	XP_016866815.1:p.Ser203=