Canonical Allele Identifier: CA2689679922

Gene: RIGI

Linked Data

• gnomAD v4: 9-32455566-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32455566_32455567insA , CM000671.2:g.32455566_32455567insA	GRCh38
NC_000009.11:g.32455564_32455565insA , CM000671.1:g.32455564_32455565insA	GRCh37
NC_000009.10:g.32445564_32445565insA	NCBI36
NG_046918.1:g.75758_75759insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379868.6:c.*1555_*1556insT	ENSP00000369197.2:n.*1555_*1556insT
ENST00000379883.3:c.*1555_*1556insT MANE Select	ENSP00000369213.2:n.*1555_*1556insT
ENST00000679665.1:c.*1555_*1556insT	ENSP00000504921.1:n.*1555_*1556insT
ENST00000679771.1:c.*3756_*3757insT	ENSP00000505015.1:n.*3756_*3757insT
ENST00000680198.1:c.*4101_*4102insT	ENSP00000505143.1:n.*4101_*4102insT
ENST00000681750.1:c.*1555_*1556insT	ENSP00000506413.1:n.*1555_*1556insT
NM_014314.3:c.*1555_*1556insT	NP_055129.2:n.*1555_*1556insT
NM_014314.4:c.*1555_*1556insT MANE Select	NP_055129.2:n.*1555_*1556insT
NM_001385907.1:c.*1555_*1556insT	NP_001372836.1:n.*1555_*1556insT
NM_001385909.1:c.*1555_*1556insT	NP_001372838.1:n.*1555_*1556insT
NM_001385910.1:c.*1555_*1556insT	NP_001372839.1:n.*1555_*1556insT
NM_001385912.1:c.*1555_*1556insT	NP_001372841.1:n.*1555_*1556insT
NM_001385913.1:c.*1555_*1556insT	NP_001372842.1:n.*1555_*1556insT
NM_001385914.1:c.*1555_*1556insT	NP_001372843.1:n.*1555_*1556insT