Canonical Allele Identifier: CA363054203

Gene: RNF39

Linked Data

• gnomAD v4: 6-30071466-T-C
• MyVariant Identifiers: chr6:g.30039243T>C (hg19) ; chr6:g.30071466T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30071466T>C , CM000668.2:g.30071466T>C	GRCh38
NC_000006.11:g.30039243T>C , CM000668.1:g.30039243T>C	GRCh37
NC_000006.10:g.30147222T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244360.8:c.704A>G MANE Select	ENSP00000244360.7:p.Asp235Gly
ENST00000244360.7:c.704A>G	ENSP00000244360.7:p.Asp235Gly
ENST00000376751.8:c.704A>G	ENSP00000365942.4:p.Asp235Gly
ENST00000244360.6:c.908A>G	ENSP00000244360.6:p.Asp303Gly
ENST00000376751.7:c.908A>G	ENSP00000365942.3:p.Asp303Gly
NM_025236.3:c.908A>G	NP_079512.2:p.Asp303Gly
NM_170769.2:c.908A>G	NP_739575.2:p.Asp303Gly
XM_017011325.1:c.449A>G	XP_016866814.1:p.Asp150Gly
NM_025236.4:c.704A>G MANE Select	NP_079512.3:p.Asp235Gly
NM_170769.3:c.704A>G	NP_739575.3:p.Asp235Gly