Canonical Allele Identifier: CA8822169

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80369833C>T , CM000679.2:g.80369833C>T	GRCh38
NC_000017.10:g.78343633C>T , CM000679.1:g.78343633C>T	GRCh37
NC_000017.9:g.75958228C>T	NCBI36
NG_031980.2:g.113973C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001256071.3:c.12391C>T (RNF213) MANE Select	NP_001243000.2:p.Arg4131Cys
ENST00000582970.6:c.12391C>T (RNF213) MANE Select	ENSP00000464087.1:p.Arg4131Cys
NM_001256071.2:c.12391C>T (RNF213)	NP_001243000.2:p.Arg4131Cys
NR_029376.1:n.241-14545G>A (RNF213-AS1)
ENST00000508628.6:c.12538C>T (RNF213)	ENSP00000425956.2:p.Arg4180Cys
ENST00000558116.5:n.1720C>T (RNF213)
ENST00000582970.5:c.12391C>T (RNF213)	ENSP00000464087.1:p.Arg4131Cys
XM_005257545.3:c.12538C>T (RNF213)	XP_005257602.2:p.Arg4180Cys
XM_005257545.4:c.12538C>T (RNF213)	XP_005257602.2:p.Arg4180Cys
XM_005257546.3:c.12538C>T (RNF213)	XP_005257603.2:p.Arg4180Cys
XM_005257546.4:c.12538C>T (RNF213)	XP_005257603.2:p.Arg4180Cys
XM_006721995.2:c.12538C>T (RNF213)	XP_006722058.1:p.Arg4180Cys
XM_006721995.3:c.12538C>T (RNF213)	XP_006722058.1:p.Arg4180Cys
XM_011525084.1:c.12538C>T (RNF213)	XP_011523386.1:p.Arg4180Cys
XM_011525084.2:c.12538C>T (RNF213)	XP_011523386.1:p.Arg4180Cys
XM_011525085.1:c.12538C>T (RNF213)	XP_011523387.1:p.Arg4180Cys
XM_011525086.1:c.12538C>T (RNF213)	XP_011523388.1:p.Arg4180Cys
XM_011525086.2:c.12538C>T (RNF213)	XP_011523388.1:p.Arg4180Cys
XM_017024905.2:c.11533C>T (RNF213)	XP_016880394.1:p.Arg3845Cys
XR_243676.3:n.12709C>T (RNF213)