Canonical Allele Identifier: CA401409004

Gene: RNF213 RNF213-AS1

Linked Data

• COSMIC: COSM4880280 ; COSM4880281
• MyVariant Identifiers: chr17:g.78341789C>G (hg19) ; chr17:g.80367989C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80367989C>G , CM000679.2:g.80367989C>G	GRCh38
NC_000017.10:g.78341789C>G , CM000679.1:g.78341789C>G	GRCh37
NC_000017.9:g.75956384C>G	NCBI36
NG_031980.2:g.112129C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12001C>G (RNF213) MANE Select	ENSP00000464087.1:p.Leu4001Val
ENST00000508628.6:c.12148C>G (RNF213)	ENSP00000425956.2:p.Leu4050Val
ENST00000558116.5:n.1330C>G (RNF213)
ENST00000582970.5:c.12001C>G (RNF213)	ENSP00000464087.1:p.Leu4001Val
NM_001256071.2:c.12001C>G (RNF213)	NP_001243000.2:p.Leu4001Val
NR_029376.1:n.241-12701G>C (RNF213-AS1)
XM_005257545.3:c.12148C>G (RNF213)	XP_005257602.2:p.Leu4050Val
XM_005257546.3:c.12148C>G (RNF213)	XP_005257603.2:p.Leu4050Val
XM_006721995.2:c.12148C>G (RNF213)	XP_006722058.1:p.Leu4050Val
XM_011525084.1:c.12148C>G (RNF213)	XP_011523386.1:p.Leu4050Val
XM_011525085.1:c.12148C>G (RNF213)	XP_011523387.1:p.Leu4050Val
XM_011525086.1:c.12148C>G (RNF213)	XP_011523388.1:p.Leu4050Val
XR_243676.3:n.12319C>G (RNF213)
XM_005257545.4:c.12148C>G (RNF213)	XP_005257602.2:p.Leu4050Val
XM_005257546.4:c.12148C>G (RNF213)	XP_005257603.2:p.Leu4050Val
XM_006721995.3:c.12148C>G (RNF213)	XP_006722058.1:p.Leu4050Val
XM_011525084.2:c.12148C>G (RNF213)	XP_011523386.1:p.Leu4050Val
XM_011525086.2:c.12148C>G (RNF213)	XP_011523388.1:p.Leu4050Val
XM_017024905.2:c.11143C>G (RNF213)	XP_016880394.1:p.Leu3715Val
NM_001256071.3:c.12001C>G (RNF213) MANE Select	NP_001243000.2:p.Leu4001Val