Human (GRCh38.p14)
Description

t-complex 11 family, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:48335]

About this transcript

This transcript has 10 exons, is annotated with 5 domains and features, is associated with 1548 variant alleles and maps to 660 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000642911.3TCP11X2-2021758502aaENSP00000496057.1
 
Protein coding
A0A2R8YGI6 NM_001405027.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1
ENST00000696789.1TCP11X2-206465951aaENSP00000512871.1
 
Nonsense mediated decay
A0A2R8Y3D8 --
ENST00000645197.1TCP11X2-204174751aaENSP00000493581.1
 
Nonsense mediated decay
A0A2R8Y3D8 --
ENST00000643059.1TCP11X2-203158451aaENSP00000495822.1
 
Nonsense mediated decay
A0A2R8Y3D8 --
ENST00000672117.1TCP11X2-2051224312aaENSP00000500149.1
 
Nonsense mediated decay
B4DZS4 --
ENST00000462555.1TCP11X2-201416No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 10, Coding exons: 9, Transcript length: 1,758 bps, Translation length: 502 residues

MANE

This MANE Select transcript contains ENSP00000496057 and matches to NM_001405027.1 and NP_001391956.1

Version

ENST00000642911.3

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Annotation Attributes

inferred transcript model [Definitions]

RNA-Seq supported partial

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.