Canonical Allele Identifier: CA1200375932
Gene: RIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155904402T= , CM000663.2:g.155904402T= GRCh38
NC_000001.10:g.155874193T= , CM000663.1:g.155874193T= GRCh37
NC_000001.9:g.154140817T= NCBI36
NG_033885.1:g.12001A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461050.6:c.*67A= ENSP00000476319.1:n.*67A=
ENST00000539040.6:c.230A= ENSP00000441950.1:p.Glu77=
ENST00000704061.1:c.*9A= ENSP00000515664.1:n.*9A=
ENST00000368323.8:c.338A= MANE Select ENSP00000357306.3:p.Glu113=
ENST00000651833.1:c.338A= ENSP00000498732.1:p.Glu113=
ENST00000651853.1:c.341A= ENSP00000498685.1:p.Glu114=
ENST00000368322.7:c.389A= ENSP00000357305.3:p.Glu130=
ENST00000368323.7:c.338A= ENSP00000357306.3:p.Glu113=
ENST00000461050.5:c.*67A= ENSP00000476319.1:n.*67A=
ENST00000539040.5:c.230A= ENSP00000441950.1:p.Glu77=
ENST00000609492.1:c.338A= ENSP00000476612.1:p.Glu113=
NM_001256820.1:c.230A= NP_001243749.1:p.Glu77=
NM_001256821.1:c.389A= NP_001243750.1:p.Glu130=
NM_006912.5:c.338A= NP_008843.1:p.Glu113=
NM_001256820.2:c.230A= NP_001243749.1:p.Glu77=
NM_001256821.2:c.389A= NP_001243750.1:p.Glu130=
NM_006912.6:c.338A= MANE Select NP_008843.1:p.Glu113=