Canonical Allele Identifier: CA2277946705

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373321_80373329delinsTCACACCCC , CM000679.2:g.80373321_80373329delinsTCACACCCC	GRCh38
NC_000017.10:g.78347121_78347129delinsTCACACCCC , CM000679.1:g.78347121_78347129delinsTCACACCCC	GRCh37
NC_000017.9:g.75961716_75961724delinsTCACACCCC	NCBI36
NG_031980.2:g.117461_117469delinsTCACACCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12942+156_12942+164delinsTCACACCCC (RNF213) MANE Select	ENSP00000464087.1:n.12942+156_12942+164delinsTCACACCCC
ENST00000411702.7:n.740+156_740+164delinsTCACACCCC (RNF213)
ENST00000508628.6:c.13089+156_13089+164delinsTCACACCCC (RNF213)	ENSP00000425956.2:n.13089+156_13089+164delinsTCACACCCC
ENST00000558116.5:n.2271+156_2271+164delinsTCACACCCC (RNF213)
ENST00000573038.1:c.97+156_97+164delinsTCACACCCC (RNF213)
ENST00000582970.5:c.12942+156_12942+164delinsTCACACCCC (RNF213)	ENSP00000464087.1:n.12942+156_12942+164delinsTCACACCCC
NM_001256071.2:c.12942+156_12942+164delinsTCACACCCC (RNF213)	NP_001243000.2:n.12942+156_12942+164delinsTCACACCCC
NR_029376.1:n.241-18041_241-18033delinsGGGGTGTGA (RNF213-AS1)
XM_005257545.3:c.13089+156_13089+164delinsTCACACCCC (RNF213)	XP_005257602.2:n.13089+156_13089+164delinsTCACACCCC
XM_005257546.3:c.13089+156_13089+164delinsTCACACCCC (RNF213)	XP_005257603.2:n.13089+156_13089+164delinsTCACACCCC
XM_006721995.2:c.13089+156_13089+164delinsTCACACCCC (RNF213)	XP_006722058.1:n.13089+156_13089+164delinsTCACACCCC
XM_011525084.1:c.13089+156_13089+164delinsTCACACCCC (RNF213)	XP_011523386.1:n.13089+156_13089+164delinsTCACACCCC
XM_011525085.1:c.13089+156_13089+164delinsTCACACCCC (RNF213)	XP_011523387.1:n.13089+156_13089+164delinsTCACACCCC
XR_243676.3:n.13260+156_13260+164delinsTCACACCCC (RNF213)
XM_005257545.4:c.13089+156_13089+164delinsTCACACCCC (RNF213)	XP_005257602.2:n.13089+156_13089+164delinsTCACACCCC
XM_005257546.4:c.13089+156_13089+164delinsTCACACCCC (RNF213)	XP_005257603.2:n.13089+156_13089+164delinsTCACACCCC
XM_006721995.3:c.13089+156_13089+164delinsTCACACCCC (RNF213)	XP_006722058.1:n.13089+156_13089+164delinsTCACACCCC
XM_011525084.2:c.13089+156_13089+164delinsTCACACCCC (RNF213)	XP_011523386.1:n.13089+156_13089+164delinsTCACACCCC
XM_017024905.2:c.12084+156_12084+164delinsTCACACCCC (RNF213)	XP_016880394.1:n.12084+156_12084+164delinsTCACACCCC
NM_001256071.3:c.12942+156_12942+164delinsTCACACCCC (RNF213) MANE Select	NP_001243000.2:n.12942+156_12942+164delinsTCACACCCC