Canonical Allele Identifier: CA502210635

Gene: RNF213 RNF213-AS1

Linked Data

• MyVariant Identifiers: chr17:g.78341899T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80368099T>A , CM000679.2:g.80368099T>A	GRCh38
NC_000017.10:g.78341899T>A , CM000679.1:g.78341899T>A	GRCh37
NC_000017.9:g.75956494T>A	NCBI36
NG_031980.2:g.112239T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12111T>A (RNF213) MANE Select	ENSP00000464087.1:p.Thr4037=
ENST00000508628.6:c.12258T>A (RNF213)	ENSP00000425956.2:p.Thr4086=
ENST00000558116.5:n.1440T>A (RNF213)
ENST00000582970.5:c.12111T>A (RNF213)	ENSP00000464087.1:p.Thr4037=
NM_001256071.2:c.12111T>A (RNF213)	NP_001243000.2:p.Thr4037=
NR_029376.1:n.241-12811A>T (RNF213-AS1)
XM_005257545.3:c.12258T>A (RNF213)	XP_005257602.2:p.Thr4086=
XM_005257546.3:c.12258T>A (RNF213)	XP_005257603.2:p.Thr4086=
XM_006721995.2:c.12258T>A (RNF213)	XP_006722058.1:p.Thr4086=
XM_011525084.1:c.12258T>A (RNF213)	XP_011523386.1:p.Thr4086=
XM_011525085.1:c.12258T>A (RNF213)	XP_011523387.1:p.Thr4086=
XM_011525086.1:c.12258T>A (RNF213)	XP_011523388.1:p.Thr4086=
XR_243676.3:n.12429T>A (RNF213)
XM_005257545.4:c.12258T>A (RNF213)	XP_005257602.2:p.Thr4086=
XM_005257546.4:c.12258T>A (RNF213)	XP_005257603.2:p.Thr4086=
XM_006721995.3:c.12258T>A (RNF213)	XP_006722058.1:p.Thr4086=
XM_011525084.2:c.12258T>A (RNF213)	XP_011523386.1:p.Thr4086=
XM_011525086.2:c.12258T>A (RNF213)	XP_011523388.1:p.Thr4086=
XM_017024905.2:c.11253T>A (RNF213)	XP_016880394.1:p.Thr3751=
NM_001256071.3:c.12111T>A (RNF213) MANE Select	NP_001243000.2:p.Thr4037=