Canonical Allele Identifier: CA2576417165

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80372968_80372969insA , CM000679.2:g.80372968_80372969insA	GRCh38
NC_000017.10:g.78346768_78346769insA , CM000679.1:g.78346768_78346769insA	GRCh37
NC_000017.9:g.75961363_75961364insA	NCBI36
NG_031980.2:g.117108_117109insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12752-7_12752-6insA (RNF213) MANE Select	ENSP00000464087.1:n.12752-7_12752-6insA
ENST00000411702.7:n.550-7_550-6insA (RNF213)
ENST00000508628.6:c.12899-7_12899-6insA (RNF213)	ENSP00000425956.2:n.12899-7_12899-6insA
ENST00000558116.5:n.2081-7_2081-6insA (RNF213)
ENST00000582970.5:c.12752-7_12752-6insA (RNF213)	ENSP00000464087.1:n.12752-7_12752-6insA
NM_001256071.2:c.12752-7_12752-6insA (RNF213)	NP_001243000.2:n.12752-7_12752-6insA
NR_029376.1:n.241-17681_241-17680insT (RNF213-AS1)
XM_005257545.3:c.12899-7_12899-6insA (RNF213)	XP_005257602.2:n.12899-7_12899-6insA
XM_005257546.3:c.12899-7_12899-6insA (RNF213)	XP_005257603.2:n.12899-7_12899-6insA
XM_006721995.2:c.12899-7_12899-6insA (RNF213)	XP_006722058.1:n.12899-7_12899-6insA
XM_011525084.1:c.12899-7_12899-6insA (RNF213)	XP_011523386.1:n.12899-7_12899-6insA
XM_011525085.1:c.12899-7_12899-6insA (RNF213)	XP_011523387.1:n.12899-7_12899-6insA
XR_243676.3:n.13070-7_13070-6insA (RNF213)
XM_005257545.4:c.12899-7_12899-6insA (RNF213)	XP_005257602.2:n.12899-7_12899-6insA
XM_005257546.4:c.12899-7_12899-6insA (RNF213)	XP_005257603.2:n.12899-7_12899-6insA
XM_006721995.3:c.12899-7_12899-6insA (RNF213)	XP_006722058.1:n.12899-7_12899-6insA
XM_011525084.2:c.12899-7_12899-6insA (RNF213)	XP_011523386.1:n.12899-7_12899-6insA
XM_017024905.2:c.11894-7_11894-6insA (RNF213)	XP_016880394.1:n.11894-7_11894-6insA
NM_001256071.3:c.12752-7_12752-6insA (RNF213) MANE Select	NP_001243000.2:n.12752-7_12752-6insA