Human (GRCh38.p14)
Description

t-complex 11 family, X-linked 1 [Source:HGNC Symbol;Acc:HGNC:48369]

Location

Chromosome X: 102,215,298-102,229,532 forward strand.

GRCh38:CM000685.2

About this gene

This gene has 5 transcripts (splice variants), 156 orthologues and 4 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000622971.4TCP11X1-2021758502aaENSP00000494553.1
 
Protein coding
A0A2R8YDF9 NM_001405026.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:NA
ENST00000597070.5TCP11X1-201174751aaENSP00000495828.1
 
Nonsense mediated decay
A0A2R8Y3D8 -TSL:2
ENST00000623912.3TCP11X1-203171551aaENSP00000495957.1
 
Nonsense mediated decay
A0A2R8Y3D8 -TSL:5
ENST00000696787.1TCP11X1-20453551aaENSP00000512870.1
 
Nonsense mediated decay
A0A2R8Y3D8 --
ENST00000696788.1TCP11X1-205573No protein-
 
Protein coding CDS not defined
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