Canonical Allele Identifier: CA1618577327

Gene: RNF39

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30072998_30072999delinsCT , CM000668.2:g.30072998_30072999delinsCT	GRCh38
NC_000006.11:g.30040775_30040776delinsCT , CM000668.1:g.30040775_30040776delinsCT	GRCh37
NC_000006.10:g.30148754_30148755delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244360.8:c.478+158_478+159delinsAG MANE Select	ENSP00000244360.7:n.478+158_478+159delinsAG
ENST00000244360.7:c.478+158_478+159delinsAG	ENSP00000244360.7:n.478+158_478+159delinsAG
ENST00000376751.8:c.478+158_478+159delinsAG	ENSP00000365942.4:n.478+158_478+159delinsAG
ENST00000244360.6:c.682+158_682+159delinsAG	ENSP00000244360.6:n.682+158_682+159delinsAG
ENST00000376751.7:c.682+158_682+159delinsAG	ENSP00000365942.3:n.682+158_682+159delinsAG
NM_025236.3:c.682+158_682+159delinsAG	NP_079512.2:n.682+158_682+159delinsAG
NM_170769.2:c.682+158_682+159delinsAG	NP_739575.2:n.682+158_682+159delinsAG
XM_017011325.1:c.223+158_223+159delinsAG	XP_016866814.1:n.223+158_223+159delinsAG
XM_017011326.1:c.682+158_682+159delinsAG	XP_016866815.1:n.682+158_682+159delinsAG
NM_025236.4:c.478+158_478+159delinsAG MANE Select	NP_079512.3:n.478+158_478+159delinsAG
NM_170769.3:c.478+158_478+159delinsAG	NP_739575.3:n.478+158_478+159delinsAG