Canonical Allele Identifier: CA1844669837

Gene: RIGI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32455797A= , CM000671.2:g.32455797A=	GRCh38
NC_000009.11:g.32455795A= , CM000671.1:g.32455795A=	GRCh37
NC_000009.10:g.32445795A=	NCBI36
NG_046918.1:g.75528T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379868.6:c.*1325T=	ENSP00000369197.2:n.*1325T=
ENST00000379883.3:c.*1325T= MANE Select	ENSP00000369213.2:n.*1325T=
ENST00000679665.1:c.*1325T=	ENSP00000504921.1:n.*1325T=
ENST00000679771.1:c.*3526T=	ENSP00000505015.1:n.*3526T=
ENST00000680198.1:c.*3871T=	ENSP00000505143.1:n.*3871T=
ENST00000681750.1:c.*1325T=	ENSP00000506413.1:n.*1325T=
ENST00000379868.5:c.*1325T=	ENSP00000369197.1:n.*1325T=
ENST00000379883.2:c.*1325T=	ENSP00000369213.2:n.*1325T=
NM_014314.3:c.*1325T=	NP_055129.2:n.*1325T=
NM_014314.4:c.*1325T= MANE Select	NP_055129.2:n.*1325T=
NM_001385907.1:c.*1325T=	NP_001372836.1:n.*1325T=
NM_001385909.1:c.*1325T=	NP_001372838.1:n.*1325T=
NM_001385910.1:c.*1325T=	NP_001372839.1:n.*1325T=
NM_001385912.1:c.*1325T=	NP_001372841.1:n.*1325T=
NM_001385913.1:c.*1325T=	NP_001372842.1:n.*1325T=
NM_001385914.1:c.*1325T=	NP_001372843.1:n.*1325T=