Canonical Allele Identifier: CA587147096

Gene: RIGI

Linked Data

• dbSNP Id: rs969528809
• gnomAD v2: 9-32455675-G-A
• MyVariant Identifiers: chr9:g.32455675G>A (hg19) ; chr9:g.32455677G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32455677G>A , CM000671.2:g.32455677G>A	GRCh38
NC_000009.11:g.32455675G>A , CM000671.1:g.32455675G>A	GRCh37
NC_000009.10:g.32445675G>A	NCBI36
NG_046918.1:g.75648C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379868.6:c.*1445C>T	ENSP00000369197.2:n.*1445C>T
ENST00000379883.3:c.*1445C>T MANE Select	ENSP00000369213.2:n.*1445C>T
ENST00000679665.1:c.*1445C>T	ENSP00000504921.1:n.*1445C>T
ENST00000679771.1:c.*3646C>T	ENSP00000505015.1:n.*3646C>T
ENST00000680198.1:c.*3991C>T	ENSP00000505143.1:n.*3991C>T
ENST00000681750.1:c.*1445C>T	ENSP00000506413.1:n.*1445C>T
NM_014314.3:c.*1445C>T	NP_055129.2:n.*1445C>T
NM_014314.4:c.*1445C>T MANE Select	NP_055129.2:n.*1445C>T
NM_001385907.1:c.*1445C>T	NP_001372836.1:n.*1445C>T
NM_001385909.1:c.*1445C>T	NP_001372838.1:n.*1445C>T
NM_001385910.1:c.*1445C>T	NP_001372839.1:n.*1445C>T
NM_001385912.1:c.*1445C>T	NP_001372841.1:n.*1445C>T
NM_001385913.1:c.*1445C>T	NP_001372842.1:n.*1445C>T
NM_001385914.1:c.*1445C>T	NP_001372843.1:n.*1445C>T