Canonical Allele Identifier: CA2277946508

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373080A= , CM000679.2:g.80373080A=	GRCh38
NC_000017.10:g.78346880A= , CM000679.1:g.78346880A=	GRCh37
NC_000017.9:g.75961475A=	NCBI36
NG_031980.2:g.117220A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12857A= (RNF213) MANE Select	ENSP00000464087.1:p.Gln4286=
ENST00000411702.7:n.655A= (RNF213)
ENST00000508628.6:c.13004A= (RNF213)	ENSP00000425956.2:p.Gln4335=
ENST00000558116.5:n.2186A= (RNF213)
ENST00000573038.1:c.12A= (RNF213)
ENST00000582970.5:c.12857A= (RNF213)	ENSP00000464087.1:p.Gln4286=
NM_001256071.2:c.12857A= (RNF213)	NP_001243000.2:p.Gln4286=
NR_029376.1:n.241-17792T= (RNF213-AS1)
XM_005257545.3:c.13004A= (RNF213)	XP_005257602.2:p.Gln4335=
XM_005257546.3:c.13004A= (RNF213)	XP_005257603.2:p.Gln4335=
XM_006721995.2:c.13004A= (RNF213)	XP_006722058.1:p.Gln4335=
XM_011525084.1:c.13004A= (RNF213)	XP_011523386.1:p.Gln4335=
XM_011525085.1:c.13004A= (RNF213)	XP_011523387.1:p.Gln4335=
XR_243676.3:n.13175A= (RNF213)
XM_005257545.4:c.13004A= (RNF213)	XP_005257602.2:p.Gln4335=
XM_005257546.4:c.13004A= (RNF213)	XP_005257603.2:p.Gln4335=
XM_006721995.3:c.13004A= (RNF213)	XP_006722058.1:p.Gln4335=
XM_011525084.2:c.13004A= (RNF213)	XP_011523386.1:p.Gln4335=
XM_017024905.2:c.11999A= (RNF213)	XP_016880394.1:p.Gln4000=
NM_001256071.3:c.12857A= (RNF213) MANE Select	NP_001243000.2:p.Gln4286=