Canonical Allele Identifier: CA863273529
Gene: RIGI HGNC NCBI

Linked Data

dbSNP Id: rs1300841181

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32455753_32455755del , CM000671.2:g.32455753_32455755del GRCh38
NC_000009.11:g.32455751_32455753del , CM000671.1:g.32455751_32455753del GRCh37
NC_000009.10:g.32445751_32445753del NCBI36
NG_046918.1:g.75578_75580del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379868.6:c.*1375_*1377del ENSP00000369197.2:n.*1375_*1377del
ENST00000379883.3:c.*1375_*1377del MANE Select ENSP00000369213.2:n.*1375_*1377del
ENST00000679665.1:c.*1375_*1377del ENSP00000504921.1:n.*1375_*1377del
ENST00000679771.1:c.*3576_*3578del ENSP00000505015.1:n.*3576_*3578del
ENST00000680198.1:c.*3921_*3923del ENSP00000505143.1:n.*3921_*3923del
ENST00000681750.1:c.*1375_*1377del ENSP00000506413.1:n.*1375_*1377del
ENST00000379868.5:c.*1375_*1377del ENSP00000369197.1:n.*1375_*1377del
ENST00000379883.2:c.*1375_*1377del ENSP00000369213.2:n.*1375_*1377del
NM_014314.3:c.*1375_*1377del NP_055129.2:n.*1375_*1377del
NM_014314.4:c.*1375_*1377del MANE Select NP_055129.2:n.*1375_*1377del
NM_001385907.1:c.*1375_*1377del NP_001372836.1:n.*1375_*1377del
NM_001385909.1:c.*1375_*1377del NP_001372838.1:n.*1375_*1377del
NM_001385910.1:c.*1375_*1377del NP_001372839.1:n.*1375_*1377del
NM_001385912.1:c.*1375_*1377del NP_001372841.1:n.*1375_*1377del
NM_001385913.1:c.*1375_*1377del NP_001372842.1:n.*1375_*1377del
NM_001385914.1:c.*1375_*1377del NP_001372843.1:n.*1375_*1377del