Canonical Allele Identifier: CA342802966

Gene: RIT1

Linked Data

• MyVariant Identifiers: chr1:g.155874289T>A (hg19) ; chr1:g.155904498T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904498T>A , CM000663.2:g.155904498T>A	GRCh38
NC_000001.10:g.155874289T>A , CM000663.1:g.155874289T>A	GRCh37
NC_000001.9:g.154140913T>A	NCBI36
NG_033885.1:g.11905A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461050.6:c.250A>T	ENSP00000476319.1:p.Ser84Cys
ENST00000539040.6:c.134A>T	ENSP00000441950.1:p.Glu45Val
ENST00000704061.1:c.219A>T	ENSP00000515664.1:p.Arg73Ser
ENST00000368323.8:c.242A>T MANE Select	ENSP00000357306.3:p.Glu81Val
ENST00000651833.1:c.242A>T	ENSP00000498732.1:p.Glu81Val
ENST00000651853.1:c.245A>T	ENSP00000498685.1:p.Glu82Val
ENST00000368322.7:c.293A>T	ENSP00000357305.3:p.Glu98Val
ENST00000368323.7:c.242A>T	ENSP00000357306.3:p.Glu81Val
ENST00000461050.5:c.250A>T	ENSP00000476319.1:p.Ser84Cys
ENST00000539040.5:c.134A>T	ENSP00000441950.1:p.Glu45Val
ENST00000609492.1:c.242A>T	ENSP00000476612.1:p.Glu81Val
NM_001256820.1:c.134A>T	NP_001243749.1:p.Glu45Val
NM_001256821.1:c.293A>T	NP_001243750.1:p.Glu98Val
NM_006912.5:c.242A>T	NP_008843.1:p.Glu81Val
NM_001256820.2:c.134A>T	NP_001243749.1:p.Glu45Val
NM_001256821.2:c.293A>T	NP_001243750.1:p.Glu98Val
NM_006912.6:c.242A>T MANE Select	NP_008843.1:p.Glu81Val