Canonical Allele Identifier: CA363054201

Gene: RNF39

Linked Data

• MyVariant Identifiers: chr6:g.30039242A>T (hg19) ; chr6:g.30071465A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30071465A>T , CM000668.2:g.30071465A>T	GRCh38
NC_000006.11:g.30039242A>T , CM000668.1:g.30039242A>T	GRCh37
NC_000006.10:g.30147221A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244360.8:c.705T>A MANE Select	ENSP00000244360.7:p.Asp235Glu
ENST00000244360.7:c.705T>A	ENSP00000244360.7:p.Asp235Glu
ENST00000376751.8:c.705T>A	ENSP00000365942.4:p.Asp235Glu
ENST00000244360.6:c.909T>A	ENSP00000244360.6:p.Asp303Glu
ENST00000376751.7:c.909T>A	ENSP00000365942.3:p.Asp303Glu
NM_025236.3:c.909T>A	NP_079512.2:p.Asp303Glu
NM_170769.2:c.909T>A	NP_739575.2:p.Asp303Glu
XM_017011325.1:c.450T>A	XP_016866814.1:p.Asp150Glu
NM_025236.4:c.705T>A MANE Select	NP_079512.3:p.Asp235Glu
NM_170769.3:c.705T>A	NP_739575.3:p.Asp235Glu