Canonical Allele Identifier: CA986751797

Gene: RNF213 RNF213-AS1

Linked Data

• dbSNP Id: rs2079590904
• gnomAD v3: 17-80373233-A-ACCCCCCTACCCTCACG
• gnomAD v4: 17-80373233-A-ACCCCCCTACCCTCACG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373248_80373249insGCCCCCCTACCCTCAC , CM000679.2:g.80373248_80373249insGCCCCCCTACCCTCAC	GRCh38
NC_000017.10:g.78347048_78347049insGCCCCCCTACCCTCAC , CM000679.1:g.78347048_78347049insGCCCCCCTACCCTCAC	GRCh37
NC_000017.9:g.75961643_75961644insGCCCCCCTACCCTCAC	NCBI36
NG_031980.2:g.117388_117389insGCCCCCCTACCCTCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12942+83_12942+84insGCCCCCCTACCCTCAC (RNF213) MANE Select	ENSP00000464087.1:n.12942+83_12942+84insGCCCCCCTACCCTCAC
ENST00000411702.7:n.740+83_740+84insGCCCCCCTACCCTCAC (RNF213)
ENST00000508628.6:c.13089+83_13089+84insGCCCCCCTACCCTCAC (RNF213)	ENSP00000425956.2:n.13089+83_13089+84insGCCCCCCTACCCTCAC
ENST00000558116.5:n.2271+83_2271+84insGCCCCCCTACCCTCAC (RNF213)
ENST00000573038.1:c.97+83_97+84insGCCCCCCTACCCTCAC (RNF213)
ENST00000582970.5:c.12942+83_12942+84insGCCCCCCTACCCTCAC (RNF213)	ENSP00000464087.1:n.12942+83_12942+84insGCCCCCCTACCCTCAC
NM_001256071.2:c.12942+83_12942+84insGCCCCCCTACCCTCAC (RNF213)	NP_001243000.2:n.12942+83_12942+84insGCCCCCCTACCCTCAC
NR_029376.1:n.241-17946_241-17945insCGTGAGGGTAGGGGGG (RNF213-AS1)
XM_005257545.3:c.13089+83_13089+84insGCCCCCCTACCCTCAC (RNF213)	XP_005257602.2:n.13089+83_13089+84insGCCCCCCTACCCTCAC
XM_005257546.3:c.13089+83_13089+84insGCCCCCCTACCCTCAC (RNF213)	XP_005257603.2:n.13089+83_13089+84insGCCCCCCTACCCTCAC
XM_006721995.2:c.13089+83_13089+84insGCCCCCCTACCCTCAC (RNF213)	XP_006722058.1:n.13089+83_13089+84insGCCCCCCTACCCTCAC
XM_011525084.1:c.13089+83_13089+84insGCCCCCCTACCCTCAC (RNF213)	XP_011523386.1:n.13089+83_13089+84insGCCCCCCTACCCTCAC
XM_011525085.1:c.13089+83_13089+84insGCCCCCCTACCCTCAC (RNF213)	XP_011523387.1:n.13089+83_13089+84insGCCCCCCTACCCTCAC
XR_243676.3:n.13260+83_13260+84insGCCCCCCTACCCTCAC (RNF213)
XM_005257545.4:c.13089+83_13089+84insGCCCCCCTACCCTCAC (RNF213)	XP_005257602.2:n.13089+83_13089+84insGCCCCCCTACCCTCAC
XM_005257546.4:c.13089+83_13089+84insGCCCCCCTACCCTCAC (RNF213)	XP_005257603.2:n.13089+83_13089+84insGCCCCCCTACCCTCAC
XM_006721995.3:c.13089+83_13089+84insGCCCCCCTACCCTCAC (RNF213)	XP_006722058.1:n.13089+83_13089+84insGCCCCCCTACCCTCAC
XM_011525084.2:c.13089+83_13089+84insGCCCCCCTACCCTCAC (RNF213)	XP_011523386.1:n.13089+83_13089+84insGCCCCCCTACCCTCAC
XM_017024905.2:c.12084+83_12084+84insGCCCCCCTACCCTCAC (RNF213)	XP_016880394.1:n.12084+83_12084+84insGCCCCCCTACCCTCAC
NM_001256071.3:c.12942+83_12942+84insGCCCCCCTACCCTCAC (RNF213) MANE Select	NP_001243000.2:n.12942+83_12942+84insGCCCCCCTACCCTCAC