Canonical Allele Identifier: CA2689679927
Gene: RIGI HGNC NCBI

Linked Data

gnomAD v4: 9-32455586-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32455586G>T , CM000671.2:g.32455586G>T GRCh38
NC_000009.11:g.32455584G>T , CM000671.1:g.32455584G>T GRCh37
NC_000009.10:g.32445584G>T NCBI36
NG_046918.1:g.75739C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379868.6:c.*1536C>A ENSP00000369197.2:n.*1536C>A
ENST00000379883.3:c.*1536C>A MANE Select ENSP00000369213.2:n.*1536C>A
ENST00000679665.1:c.*1536C>A ENSP00000504921.1:n.*1536C>A
ENST00000679771.1:c.*3737C>A ENSP00000505015.1:n.*3737C>A
ENST00000680198.1:c.*4082C>A ENSP00000505143.1:n.*4082C>A
ENST00000681750.1:c.*1536C>A ENSP00000506413.1:n.*1536C>A
NM_014314.3:c.*1536C>A NP_055129.2:n.*1536C>A
NM_014314.4:c.*1536C>A MANE Select NP_055129.2:n.*1536C>A
NM_001385907.1:c.*1536C>A NP_001372836.1:n.*1536C>A
NM_001385909.1:c.*1536C>A NP_001372838.1:n.*1536C>A
NM_001385910.1:c.*1536C>A NP_001372839.1:n.*1536C>A
NM_001385912.1:c.*1536C>A NP_001372841.1:n.*1536C>A
NM_001385913.1:c.*1536C>A NP_001372842.1:n.*1536C>A
NM_001385914.1:c.*1536C>A NP_001372843.1:n.*1536C>A
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