Human (GRCh38.p14)
Description

solute carrier family 7 member 6 opposite strand [Source:HGNC Symbol;Acc:HGNC:25807]

Gene Synonyms

FLJ13291, IWR1

Location
About this transcript

This transcript has 4 exons, is associated with 5653 variant alleles and maps to 305 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000263997.11SLC7A6OS-2014191309aaENSP00000263997.5
 
Protein coding
CCDS10865Q96CW6 NM_032178.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000568538.2SLC7A6OS-205910209aaENSP00000483575.1
 
Protein coding
A0A087X0P9 -TSL:2CDS 5' incomplete
ENST00000561590.1SLC7A6OS-202706119aaENSP00000461470.1
 
Protein coding
I3L4S1 -TSL:2CDS 5' incomplete
ENST00000568315.1SLC7A6OS-20442839aaENSP00000462436.1
 
Nonsense mediated decay
J3KSD3 -TSL:3CDS 5' incomplete
ENST00000561933.1SLC7A6OS-2034180No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 4, Coding exons: 0, Transcript length: 4,180 bps,

Transcript Support Level (TSL)

TSL:2

Version

ENST00000561933.1

Type

Retained intron

Annotation Method

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