Canonical Allele Identifier: CA401411028

Gene: RNF213 RNF213-AS1

Linked Data

• MyVariant Identifiers: chr17:g.78346931A>C (hg19) ; chr17:g.80373131A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373131A>C , CM000679.2:g.80373131A>C	GRCh38
NC_000017.10:g.78346931A>C , CM000679.1:g.78346931A>C	GRCh37
NC_000017.9:g.75961526A>C	NCBI36
NG_031980.2:g.117271A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12908A>C (RNF213) MANE Select	ENSP00000464087.1:p.Gln4303Pro
ENST00000411702.7:n.706A>C (RNF213)
ENST00000508628.6:c.13055A>C (RNF213)	ENSP00000425956.2:p.Gln4352Pro
ENST00000558116.5:n.2237A>C (RNF213)
ENST00000573038.1:c.63A>C (RNF213)
ENST00000582970.5:c.12908A>C (RNF213)	ENSP00000464087.1:p.Gln4303Pro
NM_001256071.2:c.12908A>C (RNF213)	NP_001243000.2:p.Gln4303Pro
NR_029376.1:n.241-17843T>G (RNF213-AS1)
XM_005257545.3:c.13055A>C (RNF213)	XP_005257602.2:p.Gln4352Pro
XM_005257546.3:c.13055A>C (RNF213)	XP_005257603.2:p.Gln4352Pro
XM_006721995.2:c.13055A>C (RNF213)	XP_006722058.1:p.Gln4352Pro
XM_011525084.1:c.13055A>C (RNF213)	XP_011523386.1:p.Gln4352Pro
XM_011525085.1:c.13055A>C (RNF213)	XP_011523387.1:p.Gln4352Pro
XR_243676.3:n.13226A>C (RNF213)
XM_005257545.4:c.13055A>C (RNF213)	XP_005257602.2:p.Gln4352Pro
XM_005257546.4:c.13055A>C (RNF213)	XP_005257603.2:p.Gln4352Pro
XM_006721995.3:c.13055A>C (RNF213)	XP_006722058.1:p.Gln4352Pro
XM_011525084.2:c.13055A>C (RNF213)	XP_011523386.1:p.Gln4352Pro
XM_017024905.2:c.12050A>C (RNF213)	XP_016880394.1:p.Gln4017Pro
NM_001256071.3:c.12908A>C (RNF213) MANE Select	NP_001243000.2:p.Gln4303Pro