Canonical Allele Identifier: CA1844669881
Gene: RIGI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32455832_32455837delinsACAGTT , CM000671.2:g.32455832_32455837delinsACAGTT GRCh38
NC_000009.11:g.32455830_32455835delinsACAGTT , CM000671.1:g.32455830_32455835delinsACAGTT GRCh37
NC_000009.10:g.32445830_32445835delinsACAGTT NCBI36
NG_046918.1:g.75488_75493delinsAACTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000379868.6:c.*1285_*1290delinsAACTGT ENSP00000369197.2:n.*1285_*1290delinsAACTGT
ENST00000379883.3:c.*1285_*1290delinsAACTGT MANE Select ENSP00000369213.2:n.*1285_*1290delinsAACTGT
ENST00000679665.1:c.*1285_*1290delinsAACTGT ENSP00000504921.1:n.*1285_*1290delinsAACTGT
ENST00000679771.1:c.*3486_*3491delinsAACTGT ENSP00000505015.1:n.*3486_*3491delinsAACTGT
ENST00000680198.1:c.*3831_*3836delinsAACTGT ENSP00000505143.1:n.*3831_*3836delinsAACTGT
ENST00000681750.1:c.*1285_*1290delinsAACTGT ENSP00000506413.1:n.*1285_*1290delinsAACTGT
ENST00000379868.5:c.*1285_*1290delinsAACTGT ENSP00000369197.1:n.*1285_*1290delinsAACTGT
ENST00000379883.2:c.*1285_*1290delinsAACTGT ENSP00000369213.2:n.*1285_*1290delinsAACTGT
NM_014314.3:c.*1285_*1290delinsAACTGT NP_055129.2:n.*1285_*1290delinsAACTGT
NM_014314.4:c.*1285_*1290delinsAACTGT MANE Select NP_055129.2:n.*1285_*1290delinsAACTGT
NM_001385907.1:c.*1285_*1290delinsAACTGT NP_001372836.1:n.*1285_*1290delinsAACTGT
NM_001385909.1:c.*1285_*1290delinsAACTGT NP_001372838.1:n.*1285_*1290delinsAACTGT
NM_001385910.1:c.*1285_*1290delinsAACTGT NP_001372839.1:n.*1285_*1290delinsAACTGT
NM_001385912.1:c.*1285_*1290delinsAACTGT NP_001372841.1:n.*1285_*1290delinsAACTGT
NM_001385913.1:c.*1285_*1290delinsAACTGT NP_001372842.1:n.*1285_*1290delinsAACTGT
NM_001385914.1:c.*1285_*1290delinsAACTGT NP_001372843.1:n.*1285_*1290delinsAACTGT