Canonical Allele Identifier: CA192348690

Gene: RIGI

Linked Data

• dbSNP Id: rs938007524
• MyVariant Identifiers: chr9:g.32455604T>G (hg19) ; chr9:g.32455606T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32455606T>G , CM000671.2:g.32455606T>G	GRCh38
NC_000009.11:g.32455604T>G , CM000671.1:g.32455604T>G	GRCh37
NC_000009.10:g.32445604T>G	NCBI36
NG_046918.1:g.75719A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379868.6:c.*1516A>C	ENSP00000369197.2:n.*1516A>C
ENST00000379883.3:c.*1516A>C MANE Select	ENSP00000369213.2:n.*1516A>C
ENST00000679665.1:c.*1516A>C	ENSP00000504921.1:n.*1516A>C
ENST00000679771.1:c.*3717A>C	ENSP00000505015.1:n.*3717A>C
ENST00000680198.1:c.*4062A>C	ENSP00000505143.1:n.*4062A>C
ENST00000681750.1:c.*1516A>C	ENSP00000506413.1:n.*1516A>C
NM_014314.3:c.*1516A>C	NP_055129.2:n.*1516A>C
NM_014314.4:c.*1516A>C MANE Select	NP_055129.2:n.*1516A>C
NM_001385907.1:c.*1516A>C	NP_001372836.1:n.*1516A>C
NM_001385909.1:c.*1516A>C	NP_001372838.1:n.*1516A>C
NM_001385910.1:c.*1516A>C	NP_001372839.1:n.*1516A>C
NM_001385912.1:c.*1516A>C	NP_001372841.1:n.*1516A>C
NM_001385913.1:c.*1516A>C	NP_001372842.1:n.*1516A>C
NM_001385914.1:c.*1516A>C	NP_001372843.1:n.*1516A>C