Canonical Allele Identifier: CA2677814186

Gene: RNF39

Linked Data

• gnomAD v4: 6-30073013-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30073013C>T , CM000668.2:g.30073013C>T	GRCh38
NC_000006.11:g.30040790C>T , CM000668.1:g.30040790C>T	GRCh37
NC_000006.10:g.30148769C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244360.8:c.478+144G>A MANE Select	ENSP00000244360.7:n.478+144G>A
ENST00000244360.7:c.478+144G>A	ENSP00000244360.7:n.478+144G>A
ENST00000376751.8:c.478+144G>A	ENSP00000365942.4:n.478+144G>A
ENST00000244360.6:c.682+144G>A	ENSP00000244360.6:n.682+144G>A
ENST00000376751.7:c.682+144G>A	ENSP00000365942.3:n.682+144G>A
NM_025236.3:c.682+144G>A	NP_079512.2:n.682+144G>A
NM_170769.2:c.682+144G>A	NP_739575.2:n.682+144G>A
XM_017011325.1:c.223+144G>A	XP_016866814.1:n.223+144G>A
XM_017011326.1:c.682+144G>A	XP_016866815.1:n.682+144G>A
NM_025236.4:c.478+144G>A MANE Select	NP_079512.3:n.478+144G>A
NM_170769.3:c.478+144G>A	NP_739575.3:n.478+144G>A