Canonical Allele Identifier: CA2640336062
Gene: RNF213 HGNC NCBI
RNF213-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80373288_80373345del , CM000679.2:g.80373288_80373345del GRCh38
NC_000017.10:g.78347088_78347145del , CM000679.1:g.78347088_78347145del GRCh37
NC_000017.9:g.75961683_75961740del NCBI36
NG_031980.2:g.117428_117485del

Transcript Alleles

HGVS Amino-acid Change
ENST00000582970.6:c.12942+123_12942+180del (RNF213) MANE Select ENSP00000464087.1:n.12942+123_12942+180del
ENST00000411702.7:n.740+123_740+180del (RNF213)
ENST00000508628.6:c.13089+123_13089+180del (RNF213) ENSP00000425956.2:n.13089+123_13089+180del
ENST00000558116.5:n.2271+123_2271+180del (RNF213)
ENST00000573038.1:c.97+123_97+180del (RNF213)
ENST00000582970.5:c.12942+123_12942+180del (RNF213) ENSP00000464087.1:n.12942+123_12942+180del
NM_001256071.2:c.12942+123_12942+180del (RNF213) NP_001243000.2:n.12942+123_12942+180del
NR_029376.1:n.241-18056_241-17999del (RNF213-AS1)
XM_005257545.3:c.13089+123_13089+180del (RNF213) XP_005257602.2:n.13089+123_13089+180del
XM_005257546.3:c.13089+123_13089+180del (RNF213) XP_005257603.2:n.13089+123_13089+180del
XM_006721995.2:c.13089+123_13089+180del (RNF213) XP_006722058.1:n.13089+123_13089+180del
XM_011525084.1:c.13089+123_13089+180del (RNF213) XP_011523386.1:n.13089+123_13089+180del
XM_011525085.1:c.13089+123_13089+180del (RNF213) XP_011523387.1:n.13089+123_13089+180del
XR_243676.3:n.13260+123_13260+180del (RNF213)
XM_005257545.4:c.13089+123_13089+180del (RNF213) XP_005257602.2:n.13089+123_13089+180del
XM_005257546.4:c.13089+123_13089+180del (RNF213) XP_005257603.2:n.13089+123_13089+180del
XM_006721995.3:c.13089+123_13089+180del (RNF213) XP_006722058.1:n.13089+123_13089+180del
XM_011525084.2:c.13089+123_13089+180del (RNF213) XP_011523386.1:n.13089+123_13089+180del
XM_017024905.2:c.12084+123_12084+180del (RNF213) XP_016880394.1:n.12084+123_12084+180del
NM_001256071.3:c.12942+123_12942+180del (RNF213) MANE Select NP_001243000.2:n.12942+123_12942+180del