Canonical Allele Identifier: CA2277946695

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373308_80373321delinsCCACACCTCACCCT , CM000679.2:g.80373308_80373321delinsCCACACCTCACCCT	GRCh38
NC_000017.10:g.78347108_78347121delinsCCACACCTCACCCT , CM000679.1:g.78347108_78347121delinsCCACACCTCACCCT	GRCh37
NC_000017.9:g.75961703_75961716delinsCCACACCTCACCCT	NCBI36
NG_031980.2:g.117448_117461delinsCCACACCTCACCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12942+143_12942+156delinsCCACACCTCACCCT (RNF213) MANE Select	ENSP00000464087.1:n.12942+143_12942+156delinsCCACACCTCACCCT
ENST00000411702.7:n.740+143_740+156delinsCCACACCTCACCCT (RNF213)
ENST00000508628.6:c.13089+143_13089+156delinsCCACACCTCACCCT (RNF213)	ENSP00000425956.2:n.13089+143_13089+156delinsCCACACCTCACCCT
ENST00000558116.5:n.2271+143_2271+156delinsCCACACCTCACCCT (RNF213)
ENST00000573038.1:c.97+143_97+156delinsCCACACCTCACCCT (RNF213)
ENST00000582970.5:c.12942+143_12942+156delinsCCACACCTCACCCT (RNF213)	ENSP00000464087.1:n.12942+143_12942+156delinsCCACACCTCACCCT
NM_001256071.2:c.12942+143_12942+156delinsCCACACCTCACCCT (RNF213)	NP_001243000.2:n.12942+143_12942+156delinsCCACACCTCACCCT
NR_029376.1:n.241-18033_241-18020delinsAGGGTGAGGTGTGG (RNF213-AS1)
XM_005257545.3:c.13089+143_13089+156delinsCCACACCTCACCCT (RNF213)	XP_005257602.2:n.13089+143_13089+156delinsCCACACCTCACCCT
XM_005257546.3:c.13089+143_13089+156delinsCCACACCTCACCCT (RNF213)	XP_005257603.2:n.13089+143_13089+156delinsCCACACCTCACCCT
XM_006721995.2:c.13089+143_13089+156delinsCCACACCTCACCCT (RNF213)	XP_006722058.1:n.13089+143_13089+156delinsCCACACCTCACCCT
XM_011525084.1:c.13089+143_13089+156delinsCCACACCTCACCCT (RNF213)	XP_011523386.1:n.13089+143_13089+156delinsCCACACCTCACCCT
XM_011525085.1:c.13089+143_13089+156delinsCCACACCTCACCCT (RNF213)	XP_011523387.1:n.13089+143_13089+156delinsCCACACCTCACCCT
XR_243676.3:n.13260+143_13260+156delinsCCACACCTCACCCT (RNF213)
XM_005257545.4:c.13089+143_13089+156delinsCCACACCTCACCCT (RNF213)	XP_005257602.2:n.13089+143_13089+156delinsCCACACCTCACCCT
XM_005257546.4:c.13089+143_13089+156delinsCCACACCTCACCCT (RNF213)	XP_005257603.2:n.13089+143_13089+156delinsCCACACCTCACCCT
XM_006721995.3:c.13089+143_13089+156delinsCCACACCTCACCCT (RNF213)	XP_006722058.1:n.13089+143_13089+156delinsCCACACCTCACCCT
XM_011525084.2:c.13089+143_13089+156delinsCCACACCTCACCCT (RNF213)	XP_011523386.1:n.13089+143_13089+156delinsCCACACCTCACCCT
XM_017024905.2:c.12084+143_12084+156delinsCCACACCTCACCCT (RNF213)	XP_016880394.1:n.12084+143_12084+156delinsCCACACCTCACCCT
NM_001256071.3:c.12942+143_12942+156delinsCCACACCTCACCCT (RNF213) MANE Select	NP_001243000.2:n.12942+143_12942+156delinsCCACACCTCACCCT