Canonical Allele Identifier: CA1200375966
Gene: RIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155904506G= , CM000663.2:g.155904506G= GRCh38
NC_000001.10:g.155874297G= , CM000663.1:g.155874297G= GRCh37
NC_000001.9:g.154140921G= NCBI36
NG_033885.1:g.11897C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461050.6:c.246-4C= ENSP00000476319.1:n.246-4C=
ENST00000539040.6:c.130-4C= ENSP00000441950.1:n.130-4C=
ENST00000704061.1:c.215-4C= ENSP00000515664.1:n.215-4C=
ENST00000368323.8:c.238-4C= MANE Select ENSP00000357306.3:n.238-4C=
ENST00000651833.1:c.238-4C= ENSP00000498732.1:n.238-4C=
ENST00000651853.1:c.241-4C= ENSP00000498685.1:n.241-4C=
ENST00000368322.7:c.289-4C= ENSP00000357305.3:n.289-4C=
ENST00000368323.7:c.238-4C= ENSP00000357306.3:n.238-4C=
ENST00000461050.5:c.246-4C= ENSP00000476319.1:n.246-4C=
ENST00000539040.5:c.130-4C= ENSP00000441950.1:n.130-4C=
ENST00000609492.1:c.238-4C= ENSP00000476612.1:n.238-4C=
NM_001256820.1:c.130-4C= NP_001243749.1:n.130-4C=
NM_001256821.1:c.289-4C= NP_001243750.1:n.289-4C=
NM_006912.5:c.238-4C= NP_008843.1:n.238-4C=
NM_001256820.2:c.130-4C= NP_001243749.1:n.130-4C=
NM_001256821.2:c.289-4C= NP_001243750.1:n.289-4C=
NM_006912.6:c.238-4C= MANE Select NP_008843.1:n.238-4C=