Canonical Allele Identifier: CA2840527326
Gene: RIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155900701dup , CM000663.2:g.155900701dup GRCh38
NC_000001.10:g.155870492dup , CM000663.1:g.155870492dup GRCh37
NC_000001.9:g.154137116dup NCBI36
NG_033885.1:g.15702dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000461050.6:c.*159-83dup ENSP00000476319.1:n.*159-83dup
ENST00000539040.6:c.322-83dup ENSP00000441950.1:n.322-83dup
ENST00000704061.1:c.*101-83dup ENSP00000515664.1:n.*101-83dup
ENST00000368323.8:c.430-83dup MANE Select ENSP00000357306.3:n.430-83dup
ENST00000651853.1:c.433-83dup ENSP00000498685.1:n.433-83dup
ENST00000368322.7:c.481-83dup ENSP00000357305.3:n.481-83dup
ENST00000368323.7:c.430-83dup ENSP00000357306.3:n.430-83dup
ENST00000461050.5:c.*159-83dup ENSP00000476319.1:n.*159-83dup
ENST00000539040.5:c.322-83dup ENSP00000441950.1:n.322-83dup
ENST00000609492.1:c.430-83dup ENSP00000476612.1:n.430-83dup
NM_001256820.1:c.322-83dup NP_001243749.1:n.322-83dup
NM_001256821.1:c.481-83dup NP_001243750.1:n.481-83dup
NM_006912.5:c.430-83dup NP_008843.1:n.430-83dup
NM_001256820.2:c.322-83dup NP_001243749.1:n.322-83dup
NM_001256821.2:c.481-83dup NP_001243750.1:n.481-83dup
NM_006912.6:c.430-83dup MANE Select NP_008843.1:n.430-83dup