Canonical Allele Identifier: CA353868

Gene: RIT1

Linked Data

• ClinVar Variation Id: 183406
• ClinVar RCV Id: RCV000226825 ; RCV000207338 ; RCV001731491
• dbSNP Id: rs869025194
• MyVariant Identifiers: chr1:g.155874287A>T (hg19) ; chr1:g.155904496A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904496A>T , CM000663.2:g.155904496A>T	GRCh38
NC_000001.10:g.155874287A>T , CM000663.1:g.155874287A>T	GRCh37
NC_000001.9:g.154140911A>T	NCBI36
NG_033885.1:g.11907T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461050.6:c.252T>A	ENSP00000476319.1:p.Ser84Arg
ENST00000539040.6:c.136T>A	ENSP00000441950.1:p.Phe46Ile
ENST00000704061.1:c.221T>A	ENSP00000515664.1:p.Val74Asp
ENST00000368323.8:c.244T>A MANE Select	ENSP00000357306.3:p.Phe82Ile
ENST00000651833.1:c.244T>A	ENSP00000498732.1:p.Phe82Ile
ENST00000651853.1:c.247T>A	ENSP00000498685.1:p.Phe83Ile
ENST00000368322.7:c.295T>A	ENSP00000357305.3:p.Phe99Ile
ENST00000368323.7:c.244T>A	ENSP00000357306.3:p.Phe82Ile
ENST00000461050.5:c.252T>A	ENSP00000476319.1:p.Ser84Arg
ENST00000539040.5:c.136T>A	ENSP00000441950.1:p.Phe46Ile
ENST00000609492.1:c.244T>A	ENSP00000476612.1:p.Phe82Ile
NM_001256820.1:c.136T>A	NP_001243749.1:p.Phe46Ile
NM_001256821.1:c.295T>A	NP_001243750.1:p.Phe99Ile
NM_006912.5:c.244T>A	NP_008843.1:p.Phe82Ile
NM_001256820.2:c.136T>A	NP_001243749.1:p.Phe46Ile
NM_001256821.2:c.295T>A	NP_001243750.1:p.Phe99Ile
NM_006912.6:c.244T>A MANE Select	NP_008843.1:p.Phe82Ile