Canonical Allele Identifier: CA2810594869

Gene: RNF213 RNF213-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80368005_80368009del , CM000679.2:g.80368005_80368009del	GRCh38
NC_000017.10:g.78341805_78341809del , CM000679.1:g.78341805_78341809del	GRCh37
NC_000017.9:g.75956400_75956404del	NCBI36
NG_031980.2:g.112145_112149del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582970.6:c.12017_12021del (RNF213) MANE Select	ENSP00000464087.1:p.Asp4006GlyfsTer?
ENST00000508628.6:c.12164_12168del (RNF213)	ENSP00000425956.2:p.Asp4055GlyfsTer?
ENST00000558116.5:n.1346_1350del (RNF213)
ENST00000582970.5:c.12017_12021del (RNF213)	ENSP00000464087.1:p.Asp4006GlyfsTer?
NM_001256071.2:c.12017_12021del (RNF213)	NP_001243000.2:p.Asp4006GlyfsTer?
NR_029376.1:n.241-12721_241-12717del (RNF213-AS1)
XM_005257545.3:c.12164_12168del (RNF213)	XP_005257602.2:p.Asp4055GlyfsTer?
XM_005257546.3:c.12164_12168del (RNF213)	XP_005257603.2:p.Asp4055GlyfsTer?
XM_006721995.2:c.12164_12168del (RNF213)	XP_006722058.1:p.Asp4055GlyfsTer?
XM_011525084.1:c.12164_12168del (RNF213)	XP_011523386.1:p.Asp4055GlyfsTer?
XM_011525085.1:c.12164_12168del (RNF213)	XP_011523387.1:p.Asp4055GlyfsTer?
XM_011525086.1:c.12164_12168del (RNF213)	XP_011523388.1:p.Asp4055GlyfsTer?
XR_243676.3:n.12335_12339del (RNF213)
XM_005257545.4:c.12164_12168del (RNF213)	XP_005257602.2:p.Asp4055GlyfsTer?
XM_005257546.4:c.12164_12168del (RNF213)	XP_005257603.2:p.Asp4055GlyfsTer?
XM_006721995.3:c.12164_12168del (RNF213)	XP_006722058.1:p.Asp4055GlyfsTer?
XM_011525084.2:c.12164_12168del (RNF213)	XP_011523386.1:p.Asp4055GlyfsTer?
XM_011525086.2:c.12164_12168del (RNF213)	XP_011523388.1:p.Asp4055GlyfsTer?
XM_017024905.2:c.11159_11163del (RNF213)	XP_016880394.1:p.Asp3720GlyfsTer?
NM_001256071.3:c.12017_12021del (RNF213) MANE Select	NP_001243000.2:p.Asp4006GlyfsTer?