Canonical Allele Identifier: CA401376459

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80380829A>G , CM000679.2:g.80380829A>G	GRCh38
NC_000017.10:g.78354629A>G , CM000679.1:g.78354629A>G	GRCh37
NC_000017.9:g.75969224A>G	NCBI36
NG_031980.2:g.124969A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001256071.3:c.13641-2A>G (RNF213) MANE Select	NP_001243000.2:n.13641-2A>G
ENST00000582970.6:c.13641-2A>G (RNF213) MANE Select	ENSP00000464087.1:n.13641-2A>G
NM_001256071.2:c.13641-2A>G (RNF213)	NP_001243000.2:n.13641-2A>G
NR_029376.1:n.241-25541T>C (RNF213-AS1)
ENST00000411702.7:n.1439-2A>G (RNF213)
ENST00000508628.6:c.13788-2A>G (RNF213)	ENSP00000425956.2:n.13788-2A>G
ENST00000558116.5:n.2970-2A>G (RNF213)
ENST00000572622.1:n.260-2A>G (RNF213)
ENST00000582970.5:c.13641-2A>G (RNF213)	ENSP00000464087.1:n.13641-2A>G
XM_005257545.3:c.13788-2A>G (RNF213)	XP_005257602.2:n.13788-2A>G
XM_005257545.4:c.13788-2A>G (RNF213)	XP_005257602.2:n.13788-2A>G
XM_005257546.3:c.13788-2A>G (RNF213)	XP_005257603.2:n.13788-2A>G
XM_005257546.4:c.13788-2A>G (RNF213)	XP_005257603.2:n.13788-2A>G
XM_006721995.2:c.13788-2A>G (RNF213)	XP_006722058.1:n.13788-2A>G
XM_006721995.3:c.13788-2A>G (RNF213)	XP_006722058.1:n.13788-2A>G
XM_011525084.1:c.13788-2A>G (RNF213)	XP_011523386.1:n.13788-2A>G
XM_011525084.2:c.13788-2A>G (RNF213)	XP_011523386.1:n.13788-2A>G
XM_011525085.1:c.13788-2A>G (RNF213)	XP_011523387.1:n.13788-2A>G
XM_017024905.2:c.12783-2A>G (RNF213)	XP_016880394.1:n.12783-2A>G
XR_243676.3:n.13864-2A>G (RNF213)