Canonical Allele Identifier: CA2529148713

Gene: RIGI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32455730_32455734del , CM000671.2:g.32455730_32455734del	GRCh38
NC_000009.11:g.32455728_32455732del , CM000671.1:g.32455728_32455732del	GRCh37
NC_000009.10:g.32445728_32445732del	NCBI36
NG_046918.1:g.75591_75595del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379868.6:c.*1388_*1392del	ENSP00000369197.2:n.*1388_*1392del
ENST00000379883.3:c.*1388_*1392del MANE Select	ENSP00000369213.2:n.*1388_*1392del
ENST00000679665.1:c.*1388_*1392del	ENSP00000504921.1:n.*1388_*1392del
ENST00000679771.1:c.*3589_*3593del	ENSP00000505015.1:n.*3589_*3593del
ENST00000680198.1:c.*3934_*3938del	ENSP00000505143.1:n.*3934_*3938del
ENST00000681750.1:c.*1388_*1392del	ENSP00000506413.1:n.*1388_*1392del
ENST00000379868.5:c.*1388_*1392del	ENSP00000369197.1:n.*1388_*1392del
ENST00000379883.2:c.*1388_*1392del	ENSP00000369213.2:n.*1388_*1392del
NM_014314.3:c.*1388_*1392del	NP_055129.2:n.*1388_*1392del
NM_014314.4:c.*1388_*1392del MANE Select	NP_055129.2:n.*1388_*1392del
NM_001385907.1:c.*1388_*1392del	NP_001372836.1:n.*1388_*1392del
NM_001385909.1:c.*1388_*1392del	NP_001372838.1:n.*1388_*1392del
NM_001385910.1:c.*1388_*1392del	NP_001372839.1:n.*1388_*1392del
NM_001385912.1:c.*1388_*1392del	NP_001372841.1:n.*1388_*1392del
NM_001385913.1:c.*1388_*1392del	NP_001372842.1:n.*1388_*1392del
NM_001385914.1:c.*1388_*1392del	NP_001372843.1:n.*1388_*1392del