Canonical Allele Identifier: CA1618576746

Gene: RNF39

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30071463G= , CM000668.2:g.30071463G=	GRCh38
NC_000006.11:g.30039240G= , CM000668.1:g.30039240G=	GRCh37
NC_000006.10:g.30147219G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025236.4:c.707C= MANE Select	NP_079512.3:p.Ala236=
ENST00000244360.8:c.707C= MANE Select	ENSP00000244360.7:p.Ala236=
NM_025236.3:c.911C=	NP_079512.2:p.Ala304=
NM_170769.2:c.911C=	NP_739575.2:p.Ala304=
NM_170769.3:c.707C=	NP_739575.3:p.Ala236=
ENST00000244360.6:c.911C=	ENSP00000244360.6:p.Ala304=
ENST00000244360.7:c.707C=	ENSP00000244360.7:p.Ala236=
ENST00000376751.7:c.911C=	ENSP00000365942.3:p.Ala304=
ENST00000376751.8:c.707C=	ENSP00000365942.4:p.Ala236=
XM_017011325.1:c.452C=	XP_016866814.1:p.Ala151=