Canonical Allele Identifier: CA401410851

Gene: RNF213 RNF213-AS1

Linked Data

• MyVariant Identifiers: chr17:g.78346843T>A (hg19) ; chr17:g.80373043T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373043T>A , CM000679.2:g.80373043T>A	GRCh38
NC_000017.10:g.78346843T>A , CM000679.1:g.78346843T>A	GRCh37
NC_000017.9:g.75961438T>A	NCBI36
NG_031980.2:g.117183T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12820T>A (RNF213) MANE Select	ENSP00000464087.1:p.Trp4274Arg
ENST00000411702.7:n.618T>A (RNF213)
ENST00000508628.6:c.12967T>A (RNF213)	ENSP00000425956.2:p.Trp4323Arg
ENST00000558116.5:n.2149T>A (RNF213)
ENST00000582970.5:c.12820T>A (RNF213)	ENSP00000464087.1:p.Trp4274Arg
NM_001256071.2:c.12820T>A (RNF213)	NP_001243000.2:p.Trp4274Arg
NR_029376.1:n.241-17755A>T (RNF213-AS1)
XM_005257545.3:c.12967T>A (RNF213)	XP_005257602.2:p.Trp4323Arg
XM_005257546.3:c.12967T>A (RNF213)	XP_005257603.2:p.Trp4323Arg
XM_006721995.2:c.12967T>A (RNF213)	XP_006722058.1:p.Trp4323Arg
XM_011525084.1:c.12967T>A (RNF213)	XP_011523386.1:p.Trp4323Arg
XM_011525085.1:c.12967T>A (RNF213)	XP_011523387.1:p.Trp4323Arg
XR_243676.3:n.13138T>A (RNF213)
XM_005257545.4:c.12967T>A (RNF213)	XP_005257602.2:p.Trp4323Arg
XM_005257546.4:c.12967T>A (RNF213)	XP_005257603.2:p.Trp4323Arg
XM_006721995.3:c.12967T>A (RNF213)	XP_006722058.1:p.Trp4323Arg
XM_011525084.2:c.12967T>A (RNF213)	XP_011523386.1:p.Trp4323Arg
XM_017024905.2:c.11962T>A (RNF213)	XP_016880394.1:p.Trp3988Arg
NM_001256071.3:c.12820T>A (RNF213) MANE Select	NP_001243000.2:p.Trp4274Arg