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Human (GRCh38.p14)
Description

Ras related GTP binding B [Source:HGNC Symbol;Acc:HGNC:19901]

Location

Chromosome X: 55,717,743-55,758,774 forward strand.

GRCh38:CM000685.2

About this gene

This gene has 12 transcripts (splice variants), 193 orthologues and 3 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000374941.9RRAGB-2022051346aaENSP00000364077.4
 
Protein coding
CCDS14371Q5VZM2-2 NM_006064.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000959780.1RRAGB-2112224406aaENSP00000629839.1
 
Protein coding
--GENCODE Basic
ENST00000892762.1RRAGB-2072082359aaENSP00000562821.1
 
Protein coding
--GENCODE Basic
ENST00000959779.1RRAGB-2102029340aaENSP00000629838.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000959781.1RRAGB-2122022345aaENSP00000629840.1
 
Protein coding
--GENCODE Basic
ENST00000922547.1RRAGB-2081961314aaENSP00000592606.1
 
Protein coding
--GENCODE Basic
ENST00000922548.1RRAGB-2091812273aaENSP00000592607.1
 
Protein coding
--GENCODE Basic
ENST00000262850.7RRAGB-2011573374aaENSP00000262850.7
 
Protein coding
CCDS14372Q5VZM2-1 -GENCODE BasicAPPRIS P1TSL:1
ENST00000414239.5RRAGB-203644194aaENSP00000410630.1
 
Protein coding
Q5VZM0 -TSL:5CDS 3' incomplete
ENST00000474757.1RRAGB-204709No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000498762.1RRAGB-206507No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000475061.1RRAGB-205376No protein-
 
Protein coding CDS not defined
--TSL:2