Canonical Allele Identifier: CA1200375921

Gene: RIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904371A= , CM000663.2:g.155904371A=	GRCh38
NC_000001.10:g.155874162A= , CM000663.1:g.155874162A=	GRCh37
NC_000001.9:g.154140786A=	NCBI36
NG_033885.1:g.12032T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.*98T=	ENSP00000476319.1:n.*98T=
ENST00000539040.6:c.261T=	ENSP00000441950.1:p.Arg87=
ENST00000704061.1:c.*40T=	ENSP00000515664.1:n.*40T=
ENST00000368323.8:c.369T= MANE Select	ENSP00000357306.3:p.Arg123=
ENST00000651853.1:c.372T=	ENSP00000498685.1:p.Arg124=
ENST00000368322.7:c.420T=	ENSP00000357305.3:p.Arg140=
ENST00000368323.7:c.369T=	ENSP00000357306.3:p.Arg123=
ENST00000461050.5:c.*98T=	ENSP00000476319.1:n.*98T=
ENST00000539040.5:c.261T=	ENSP00000441950.1:p.Arg87=
ENST00000609492.1:c.369T=	ENSP00000476612.1:p.Arg123=
NM_001256820.1:c.261T=	NP_001243749.1:p.Arg87=
NM_001256821.1:c.420T=	NP_001243750.1:p.Arg140=
NM_006912.5:c.369T=	NP_008843.1:p.Arg123=
NM_001256820.2:c.261T=	NP_001243749.1:p.Arg87=
NM_001256821.2:c.420T=	NP_001243750.1:p.Arg140=
NM_006912.6:c.369T= MANE Select	NP_008843.1:p.Arg123=