Canonical Allele Identifier: CA2677814188

Gene: RNF39

Linked Data

• gnomAD v4: 6-30073016-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30073016A>C , CM000668.2:g.30073016A>C	GRCh38
NC_000006.11:g.30040793A>C , CM000668.1:g.30040793A>C	GRCh37
NC_000006.10:g.30148772A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244360.8:c.478+141T>G MANE Select	ENSP00000244360.7:n.478+141T>G
ENST00000244360.7:c.478+141T>G	ENSP00000244360.7:n.478+141T>G
ENST00000376751.8:c.478+141T>G	ENSP00000365942.4:n.478+141T>G
ENST00000244360.6:c.682+141T>G	ENSP00000244360.6:n.682+141T>G
ENST00000376751.7:c.682+141T>G	ENSP00000365942.3:n.682+141T>G
NM_025236.3:c.682+141T>G	NP_079512.2:n.682+141T>G
NM_170769.2:c.682+141T>G	NP_739575.2:n.682+141T>G
XM_017011325.1:c.223+141T>G	XP_016866814.1:n.223+141T>G
XM_017011326.1:c.682+141T>G	XP_016866815.1:n.682+141T>G
NM_025236.4:c.478+141T>G MANE Select	NP_079512.3:n.478+141T>G
NM_170769.3:c.478+141T>G	NP_739575.3:n.478+141T>G