Canonical Allele Identifier: CA2277946654

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373266_80373295delinsCCCCACCCCCTCACACCTTCCCCACCACAT , CM000679.2:g.80373266_80373295delinsCCCCACCCCCTCACACCTTCCCCACCACAT	GRCh38
NC_000017.10:g.78347066_78347095delinsCCCCACCCCCTCACACCTTCCCCACCACAT , CM000679.1:g.78347066_78347095delinsCCCCACCCCCTCACACCTTCCCCACCACAT	GRCh37
NC_000017.9:g.75961661_75961690delinsCCCCACCCCCTCACACCTTCCCCACCACAT	NCBI36
NG_031980.2:g.117406_117435delinsCCCCACCCCCTCACACCTTCCCCACCACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12942+101_12942+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213) MANE Select	ENSP00000464087.1:n.12942+101_12942+130delinsCCCCACCCCCTCACAC...
ENST00000411702.7:n.740+101_740+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)
ENST00000508628.6:c.13089+101_13089+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	ENSP00000425956.2:n.13089+101_13089+130delinsCCCCACCCCCTCACAC...
ENST00000558116.5:n.2271+101_2271+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)
ENST00000573038.1:c.97+101_97+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)
ENST00000582970.5:c.12942+101_12942+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	ENSP00000464087.1:n.12942+101_12942+130delinsCCCCACCCCCTCACAC...
NM_001256071.2:c.12942+101_12942+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	NP_001243000.2:n.12942+101_12942+130delinsCCCCACCCCCTCACACCTT...
NR_029376.1:n.241-18007_241-17978delinsATGTGGTGGGGAAGGTGTGAGGGGGTGGGG (RNF213-AS1)
XM_005257545.3:c.13089+101_13089+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	XP_005257602.2:n.13089+101_13089+130delinsCCCCACCCCCTCACACCTT...
XM_005257546.3:c.13089+101_13089+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	XP_005257603.2:n.13089+101_13089+130delinsCCCCACCCCCTCACACCTT...
XM_006721995.2:c.13089+101_13089+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	XP_006722058.1:n.13089+101_13089+130delinsCCCCACCCCCTCACACCTT...
XM_011525084.1:c.13089+101_13089+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	XP_011523386.1:n.13089+101_13089+130delinsCCCCACCCCCTCACACCTT...
XM_011525085.1:c.13089+101_13089+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	XP_011523387.1:n.13089+101_13089+130delinsCCCCACCCCCTCACACCTT...
XR_243676.3:n.13260+101_13260+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)
XM_005257545.4:c.13089+101_13089+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	XP_005257602.2:n.13089+101_13089+130delinsCCCCACCCCCTCACACCTT...
XM_005257546.4:c.13089+101_13089+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	XP_005257603.2:n.13089+101_13089+130delinsCCCCACCCCCTCACACCTT...
XM_006721995.3:c.13089+101_13089+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	XP_006722058.1:n.13089+101_13089+130delinsCCCCACCCCCTCACACCTT...
XM_011525084.2:c.13089+101_13089+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	XP_011523386.1:n.13089+101_13089+130delinsCCCCACCCCCTCACACCTT...
XM_017024905.2:c.12084+101_12084+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213)	XP_016880394.1:n.12084+101_12084+130delinsCCCCACCCCCTCACACCTT...
NM_001256071.3:c.12942+101_12942+130delinsCCCCACCCCCTCACACCTTCCCCACCACAT (RNF213) MANE Select	NP_001243000.2:n.12942+101_12942+130delinsCCCCACCCCCTCACACCTT...