Canonical Allele Identifier: CA1148263457
Gene: RIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155904399A= , CM000663.2:g.155904399A= GRCh38
NC_000001.10:g.155874190A= , CM000663.1:g.155874190A= GRCh37
NC_000001.9:g.154140814A= NCBI36
NG_033885.1:g.12004T=

Transcript Alleles

HGVS Amino-acid change
ENST00000461050.6:c.*70T= ENSP00000476319.1:n.*70T=
ENST00000539040.6:c.233T= ENSP00000441950.1:p.Phe78=
ENST00000704061.1:c.*12T= ENSP00000515664.1:n.*12T=
ENST00000368323.8:c.341T= MANE Select ENSP00000357306.3:p.Phe114=
ENST00000651833.1:c.341T= ENSP00000498732.1:p.Phe114=
ENST00000651853.1:c.344T= ENSP00000498685.1:p.Phe115=
ENST00000368322.7:c.392T= ENSP00000357305.3:p.Phe131=
ENST00000368323.7:c.341T= ENSP00000357306.3:p.Phe114=
ENST00000461050.5:c.*70T= ENSP00000476319.1:n.*70T=
ENST00000539040.5:c.233T= ENSP00000441950.1:p.Phe78=
ENST00000609492.1:c.341T= ENSP00000476612.1:p.Phe114=
NM_001256820.1:c.233T= NP_001243749.1:p.Phe78=
NM_001256821.1:c.392T= NP_001243750.1:p.Phe131=
NM_006912.5:c.341T= NP_008843.1:p.Phe114=
NM_001256820.2:c.233T= NP_001243749.1:p.Phe78=
NM_001256821.2:c.392T= NP_001243750.1:p.Phe131=
NM_006912.6:c.341T= MANE Select NP_008843.1:p.Phe114=