Canonical Allele Identifier: CA294936041

Gene: RNF213 RNF213-AS1

Linked Data

• dbSNP Id: rs1017631860
• gnomAD v4: 17-80373128-A-C
• MyVariant Identifiers: chr17:g.78346928A>C (hg19) ; chr17:g.80373128A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80373128A>C , CM000679.2:g.80373128A>C	GRCh38
NC_000017.10:g.78346928A>C , CM000679.1:g.78346928A>C	GRCh37
NC_000017.9:g.75961523A>C	NCBI36
NG_031980.2:g.117268A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12905A>C (RNF213) MANE Select	ENSP00000464087.1:p.His4302Pro
ENST00000411702.7:n.703A>C (RNF213)
ENST00000508628.6:c.13052A>C (RNF213)	ENSP00000425956.2:p.His4351Pro
ENST00000558116.5:n.2234A>C (RNF213)
ENST00000573038.1:c.60A>C (RNF213)
ENST00000582970.5:c.12905A>C (RNF213)	ENSP00000464087.1:p.His4302Pro
NM_001256071.2:c.12905A>C (RNF213)	NP_001243000.2:p.His4302Pro
NR_029376.1:n.241-17840T>G (RNF213-AS1)
XM_005257545.3:c.13052A>C (RNF213)	XP_005257602.2:p.His4351Pro
XM_005257546.3:c.13052A>C (RNF213)	XP_005257603.2:p.His4351Pro
XM_006721995.2:c.13052A>C (RNF213)	XP_006722058.1:p.His4351Pro
XM_011525084.1:c.13052A>C (RNF213)	XP_011523386.1:p.His4351Pro
XM_011525085.1:c.13052A>C (RNF213)	XP_011523387.1:p.His4351Pro
XR_243676.3:n.13223A>C (RNF213)
XM_005257545.4:c.13052A>C (RNF213)	XP_005257602.2:p.His4351Pro
XM_005257546.4:c.13052A>C (RNF213)	XP_005257603.2:p.His4351Pro
XM_006721995.3:c.13052A>C (RNF213)	XP_006722058.1:p.His4351Pro
XM_011525084.2:c.13052A>C (RNF213)	XP_011523386.1:p.His4351Pro
XM_017024905.2:c.12047A>C (RNF213)	XP_016880394.1:p.His4016Pro
NM_001256071.3:c.12905A>C (RNF213) MANE Select	NP_001243000.2:p.His4302Pro