Canonical Allele Identifier: CA1200375962
Gene: RIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155904501G= , CM000663.2:g.155904501G= GRCh38
NC_000001.10:g.155874292G= , CM000663.1:g.155874292G= GRCh37
NC_000001.9:g.154140916G= NCBI36
NG_033885.1:g.11902C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461050.6:c.247C= ENSP00000476319.1:p.Gln83=
ENST00000539040.6:c.131C= ENSP00000441950.1:p.Ala44=
ENST00000704061.1:c.216C= ENSP00000515664.1:p.Gly72=
ENST00000368323.8:c.239C= MANE Select ENSP00000357306.3:p.Ala80=
ENST00000651833.1:c.239C= ENSP00000498732.1:p.Ala80=
ENST00000651853.1:c.242C= ENSP00000498685.1:p.Ala81=
ENST00000368322.7:c.290C= ENSP00000357305.3:p.Ala97=
ENST00000368323.7:c.239C= ENSP00000357306.3:p.Ala80=
ENST00000461050.5:c.247C= ENSP00000476319.1:p.Gln83=
ENST00000539040.5:c.131C= ENSP00000441950.1:p.Ala44=
ENST00000609492.1:c.239C= ENSP00000476612.1:p.Ala80=
NM_001256820.1:c.131C= NP_001243749.1:p.Ala44=
NM_001256821.1:c.290C= NP_001243750.1:p.Ala97=
NM_006912.5:c.239C= NP_008843.1:p.Ala80=
NM_001256820.2:c.131C= NP_001243749.1:p.Ala44=
NM_001256821.2:c.290C= NP_001243750.1:p.Ala97=
NM_006912.6:c.239C= MANE Select NP_008843.1:p.Ala80=