Canonical Allele Identifier: CA2277946623

Gene: RNF213 RNF213-AS1

Linked Data

• dbSNP Id: rs2079593001
• gnomAD v4: 17-80373249-A-ACCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373251_80373252insTCC , CM000679.2:g.80373251_80373252insTCC	GRCh38
NC_000017.10:g.78347051_78347052insTCC , CM000679.1:g.78347051_78347052insTCC	GRCh37
NC_000017.9:g.75961646_75961647insTCC	NCBI36
NG_031980.2:g.117391_117392insTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12942+86_12942+87insTCC (RNF213) MANE Select	ENSP00000464087.1:n.12942+86_12942+87insTCC
ENST00000411702.7:n.740+86_740+87insTCC (RNF213)
ENST00000508628.6:c.13089+86_13089+87insTCC (RNF213)	ENSP00000425956.2:n.13089+86_13089+87insTCC
ENST00000558116.5:n.2271+86_2271+87insTCC (RNF213)
ENST00000573038.1:c.97+86_97+87insTCC (RNF213)
ENST00000582970.5:c.12942+86_12942+87insTCC (RNF213)	ENSP00000464087.1:n.12942+86_12942+87insTCC
NM_001256071.2:c.12942+86_12942+87insTCC (RNF213)	NP_001243000.2:n.12942+86_12942+87insTCC
NR_029376.1:n.241-17962_241-17961insAGG (RNF213-AS1)
XM_005257545.3:c.13089+86_13089+87insTCC (RNF213)	XP_005257602.2:n.13089+86_13089+87insTCC
XM_005257546.3:c.13089+86_13089+87insTCC (RNF213)	XP_005257603.2:n.13089+86_13089+87insTCC
XM_006721995.2:c.13089+86_13089+87insTCC (RNF213)	XP_006722058.1:n.13089+86_13089+87insTCC
XM_011525084.1:c.13089+86_13089+87insTCC (RNF213)	XP_011523386.1:n.13089+86_13089+87insTCC
XM_011525085.1:c.13089+86_13089+87insTCC (RNF213)	XP_011523387.1:n.13089+86_13089+87insTCC
XR_243676.3:n.13260+86_13260+87insTCC (RNF213)
XM_005257545.4:c.13089+86_13089+87insTCC (RNF213)	XP_005257602.2:n.13089+86_13089+87insTCC
XM_005257546.4:c.13089+86_13089+87insTCC (RNF213)	XP_005257603.2:n.13089+86_13089+87insTCC
XM_006721995.3:c.13089+86_13089+87insTCC (RNF213)	XP_006722058.1:n.13089+86_13089+87insTCC
XM_011525084.2:c.13089+86_13089+87insTCC (RNF213)	XP_011523386.1:n.13089+86_13089+87insTCC
XM_017024905.2:c.12084+86_12084+87insTCC (RNF213)	XP_016880394.1:n.12084+86_12084+87insTCC
NM_001256071.3:c.12942+86_12942+87insTCC (RNF213) MANE Select	NP_001243000.2:n.12942+86_12942+87insTCC