Canonical Allele Identifier: CA1200375933
Gene: RIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155904405C= , CM000663.2:g.155904405C= GRCh38
NC_000001.10:g.155874196C= , CM000663.1:g.155874196C= GRCh37
NC_000001.9:g.154140820C= NCBI36
NG_033885.1:g.11998G=

Transcript Alleles

HGVS Amino-acid change
ENST00000461050.6:c.*64G= ENSP00000476319.1:n.*64G=
ENST00000539040.6:c.227G= ENSP00000441950.1:p.Arg76=
ENST00000704061.1:c.*6G= ENSP00000515664.1:n.*6G=
ENST00000368323.8:c.335G= MANE Select ENSP00000357306.3:p.Arg112=
ENST00000651833.1:c.335G= ENSP00000498732.1:p.Arg112=
ENST00000651853.1:c.338G= ENSP00000498685.1:p.Arg113=
ENST00000368322.7:c.386G= ENSP00000357305.3:p.Arg129=
ENST00000368323.7:c.335G= ENSP00000357306.3:p.Arg112=
ENST00000461050.5:c.*64G= ENSP00000476319.1:n.*64G=
ENST00000539040.5:c.227G= ENSP00000441950.1:p.Arg76=
ENST00000609492.1:c.335G= ENSP00000476612.1:p.Arg112=
NM_001256820.1:c.227G= NP_001243749.1:p.Arg76=
NM_001256821.1:c.386G= NP_001243750.1:p.Arg129=
NM_006912.5:c.335G= NP_008843.1:p.Arg112=
NM_001256820.2:c.227G= NP_001243749.1:p.Arg76=
NM_001256821.2:c.386G= NP_001243750.1:p.Arg129=
NM_006912.6:c.335G= MANE Select NP_008843.1:p.Arg112=