Canonical Allele Identifier: CA2277943886

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80368171_80368186delinsATCCTTTTTTTCATTT , CM000679.2:g.80368171_80368186delinsATCCTTTTTTTCATTT	GRCh38
NC_000017.10:g.78341971_78341986delinsATCCTTTTTTTCATTT , CM000679.1:g.78341971_78341986delinsATCCTTTTTTTCATTT	GRCh37
NC_000017.9:g.75956566_75956581delinsATCCTTTTTTTCATTT	NCBI36
NG_031980.2:g.112311_112326delinsATCCTTTTTTTCATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12155+28_12155+43delinsATCCTTTTTTTCATTT (RNF213) MANE Select	ENSP00000464087.1:n.12155+28_12155+43delinsATCCTTTTTTTCATTT
ENST00000508628.6:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	ENSP00000425956.2:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
ENST00000558116.5:n.1484+28_1484+43delinsATCCTTTTTTTCATTT (RNF213)
ENST00000582970.5:c.12155+28_12155+43delinsATCCTTTTTTTCATTT (RNF213)	ENSP00000464087.1:n.12155+28_12155+43delinsATCCTTTTTTTCATTT
NM_001256071.2:c.12155+28_12155+43delinsATCCTTTTTTTCATTT (RNF213)	NP_001243000.2:n.12155+28_12155+43delinsATCCTTTTTTTCATTT
NR_029376.1:n.241-12898_241-12883delinsAAATGAAAAAAAGGAT (RNF213-AS1)
XM_005257545.3:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_005257602.2:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XM_005257546.3:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_005257603.2:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XM_006721995.2:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_006722058.1:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XM_011525084.1:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_011523386.1:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XM_011525085.1:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_011523387.1:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XM_011525086.1:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_011523388.1:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XR_243676.3:n.12473+28_12473+43delinsATCCTTTTTTTCATTT (RNF213)
XM_005257545.4:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_005257602.2:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XM_005257546.4:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_005257603.2:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XM_006721995.3:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_006722058.1:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XM_011525084.2:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_011523386.1:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XM_011525086.2:c.12302+28_12302+43delinsATCCTTTTTTTCATTT (RNF213)	XP_011523388.1:n.12302+28_12302+43delinsATCCTTTTTTTCATTT
XM_017024905.2:c.11297+28_11297+43delinsATCCTTTTTTTCATTT (RNF213)	XP_016880394.1:n.11297+28_11297+43delinsATCCTTTTTTTCATTT
NM_001256071.3:c.12155+28_12155+43delinsATCCTTTTTTTCATTT (RNF213) MANE Select	NP_001243000.2:n.12155+28_12155+43delinsATCCTTTTTTTCATTT