Canonical Allele Identifier: CA2277946558

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373159G= , CM000679.2:g.80373159G=	GRCh38
NC_000017.10:g.78346959G= , CM000679.1:g.78346959G=	GRCh37
NC_000017.9:g.75961554G=	NCBI36
NG_031980.2:g.117299G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12936G= (RNF213) MANE Select	ENSP00000464087.1:p.Lys4312=
ENST00000411702.7:n.734G= (RNF213)
ENST00000508628.6:c.13083G= (RNF213)	ENSP00000425956.2:p.Lys4361=
ENST00000558116.5:n.2265G= (RNF213)
ENST00000573038.1:c.91G= (RNF213)
ENST00000582970.5:c.12936G= (RNF213)	ENSP00000464087.1:p.Lys4312=
NM_001256071.2:c.12936G= (RNF213)	NP_001243000.2:p.Lys4312=
NR_029376.1:n.241-17871C= (RNF213-AS1)
XM_005257545.3:c.13083G= (RNF213)	XP_005257602.2:p.Lys4361=
XM_005257546.3:c.13083G= (RNF213)	XP_005257603.2:p.Lys4361=
XM_006721995.2:c.13083G= (RNF213)	XP_006722058.1:p.Lys4361=
XM_011525084.1:c.13083G= (RNF213)	XP_011523386.1:p.Lys4361=
XM_011525085.1:c.13083G= (RNF213)	XP_011523387.1:p.Lys4361=
XR_243676.3:n.13254G= (RNF213)
XM_005257545.4:c.13083G= (RNF213)	XP_005257602.2:p.Lys4361=
XM_005257546.4:c.13083G= (RNF213)	XP_005257603.2:p.Lys4361=
XM_006721995.3:c.13083G= (RNF213)	XP_006722058.1:p.Lys4361=
XM_011525084.2:c.13083G= (RNF213)	XP_011523386.1:p.Lys4361=
XM_017024905.2:c.12078G= (RNF213)	XP_016880394.1:p.Lys4026=
NM_001256071.3:c.12936G= (RNF213) MANE Select	NP_001243000.2:p.Lys4312=