Human (GRCh37.p13)
Description

solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1 [Source:HGNC Symbol;Acc:11075]

Gene Synonyms

EBP50, NHERF, NHERF-1, NHERF1, NPHLOP2

Location
About this transcript

This transcript has 6 exons, is annotated with 17 domains and features, is associated with 9569 variant alleles and maps to 405 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000262613.5SLC9A3R1-0011969358aaENSP00000262613.5
 
Protein coding
CCDS11705B3KY21 O14745 NM_004252.4GENCODE basic
ENST00000413388.2SLC9A3R1-0021285202aaENSP00000464982.1
 
Protein coding
B3KY21 -GENCODE basic
ENST00000583369.1SLC9A3R1-006841215aaENSP00000464321.1
 
Protein coding
J3QRP6 -CDS 3' incomplete
ENST00000581356.1SLC9A3R1-00551935aaENSP00000464117.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000578958.1SLC9A3R1-004714No protein-
 
Retained intron
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Statistics

Exons: 6, Coding exons: 6, Transcript length: 1,969 bps, Translation length: 358 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: O14745

CCDS

This transcript is a member of the Human CCDS set: CCDS11705

Version

ENST00000262613.5

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.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000443671 (version 1)
GENCODE basic gene

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