Human (GRCh38.p14)
Description

solute carrier family 9 member A1 [Source:HGNC Symbol;Acc:HGNC:11071]

Gene Synonyms

APNH, NHE-1, NHE1, PPP1R143

Location
About this transcript

This transcript has 12 exons, is annotated with 65 domains and features, is associated with 24178 variant alleles and maps to 687 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000263980.8SLC9A1-2014737815aaENSP00000263980.3
 
Protein coding
CCDS295P19634-1 NM_003047.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000374086.3SLC9A1-2032183555aaENSP00000363199.3
 
Protein coding
P19634-2 -GENCODE basicTSL:1
ENST00000374084.2SLC9A1-202695135aaENSP00000363197.2
 
Protein coding
B1ALD5 -TSL:5CDS 3' incomplete
ENST00000490329.1SLC9A1-206660No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000374089.5SLC9A1-2043165No protein-
 
Retained intron
--TSL:2
ENST00000447808.1SLC9A1-205887No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 12, Coding exons: 12, Transcript length: 4,737 bps, Translation length: 815 residues

MANE

This MANE Select transcript contains ENSP00000263980 and matches to NM_003047.5 and NP_003038.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P19634

CCDS

This transcript is a member of the Human CCDS set: CCDS295

Transcript Support Level (TSL)

TSL:1

Version

ENST00000263980.8

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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