Canonical Allele Identifier: CA2277946747

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373388_80373404delinsAGCATCCCCAGAGCCAG , CM000679.2:g.80373388_80373404delinsAGCATCCCCAGAGCCAG	GRCh38
NC_000017.10:g.78347188_78347204delinsAGCATCCCCAGAGCCAG , CM000679.1:g.78347188_78347204delinsAGCATCCCCAGAGCCAG	GRCh37
NC_000017.9:g.75961783_75961799delinsAGCATCCCCAGAGCCAG	NCBI36
NG_031980.2:g.117528_117544delinsAGCATCCCCAGAGCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12942+223_12942+239delinsAGCATCCCCAGAGCCAG (RNF213) MANE Select	ENSP00000464087.1:n.12942+223_12942+239delinsAGCATCCCCAGAGCCA...
ENST00000411702.7:n.740+223_740+239delinsAGCATCCCCAGAGCCAG (RNF213)
ENST00000508628.6:c.13089+223_13089+239delinsAGCATCCCCAGAGCCAG (RNF213)	ENSP00000425956.2:n.13089+223_13089+239delinsAGCATCCCCAGAGCCA...
ENST00000558116.5:n.2271+223_2271+239delinsAGCATCCCCAGAGCCAG (RNF213)
ENST00000573038.1:c.97+223_97+239delinsAGCATCCCCAGAGCCAG (RNF213)
ENST00000582970.5:c.12942+223_12942+239delinsAGCATCCCCAGAGCCAG (RNF213)	ENSP00000464087.1:n.12942+223_12942+239delinsAGCATCCCCAGAGCCA...
NM_001256071.2:c.12942+223_12942+239delinsAGCATCCCCAGAGCCAG (RNF213)	NP_001243000.2:n.12942+223_12942+239delinsAGCATCCCCAGAGCCAG
NR_029376.1:n.241-18116_241-18100delinsCTGGCTCTGGGGATGCT (RNF213-AS1)
XM_005257545.3:c.13089+223_13089+239delinsAGCATCCCCAGAGCCAG (RNF213)	XP_005257602.2:n.13089+223_13089+239delinsAGCATCCCCAGAGCCAG
XM_005257546.3:c.13089+223_13089+239delinsAGCATCCCCAGAGCCAG (RNF213)	XP_005257603.2:n.13089+223_13089+239delinsAGCATCCCCAGAGCCAG
XM_006721995.2:c.13089+223_13089+239delinsAGCATCCCCAGAGCCAG (RNF213)	XP_006722058.1:n.13089+223_13089+239delinsAGCATCCCCAGAGCCAG
XM_011525084.1:c.13089+223_13089+239delinsAGCATCCCCAGAGCCAG (RNF213)	XP_011523386.1:n.13089+223_13089+239delinsAGCATCCCCAGAGCCAG
XM_011525085.1:c.13089+223_13089+239delinsAGCATCCCCAGAGCCAG (RNF213)	XP_011523387.1:n.13089+223_13089+239delinsAGCATCCCCAGAGCCAG
XR_243676.3:n.13260+223_13260+239delinsAGCATCCCCAGAGCCAG (RNF213)
XM_005257545.4:c.13089+223_13089+239delinsAGCATCCCCAGAGCCAG (RNF213)	XP_005257602.2:n.13089+223_13089+239delinsAGCATCCCCAGAGCCAG
XM_005257546.4:c.13089+223_13089+239delinsAGCATCCCCAGAGCCAG (RNF213)	XP_005257603.2:n.13089+223_13089+239delinsAGCATCCCCAGAGCCAG
XM_006721995.3:c.13089+223_13089+239delinsAGCATCCCCAGAGCCAG (RNF213)	XP_006722058.1:n.13089+223_13089+239delinsAGCATCCCCAGAGCCAG
XM_011525084.2:c.13089+223_13089+239delinsAGCATCCCCAGAGCCAG (RNF213)	XP_011523386.1:n.13089+223_13089+239delinsAGCATCCCCAGAGCCAG
XM_017024905.2:c.12084+223_12084+239delinsAGCATCCCCAGAGCCAG (RNF213)	XP_016880394.1:n.12084+223_12084+239delinsAGCATCCCCAGAGCCAG
NM_001256071.3:c.12942+223_12942+239delinsAGCATCCCCAGAGCCAG (RNF213) MANE Select	NP_001243000.2:n.12942+223_12942+239delinsAGCATCCCCAGAGCCAG