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Human (GRCh38.p14)
Description

spectrin beta, non-erythrocytic 4 [Source:HGNC Symbol;Acc:HGNC:14896]

Gene Synonyms

KIAA1642, SPTBN3

Location

Chromosome 19: 40,466,241-40,576,464 forward strand.

GRCh38:CM000681.2

About this gene

This gene has 12 transcripts (splice variants), 268 orthologues, 36 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000598249.6SPTBN4-21089102564aaENSP00000469242.1
 
Protein coding
CCDS12559Q9H254-1 NM_020971.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000352632.7SPTBN4-20186762564aaENSP00000263373.2
 
Protein coding
CCDS12559Q9H254-1 -GENCODE BasicAPPRIS P1TSL:5
ENST00000595535.5SPTBN4-20561052002aaENSP00000470693.1
 
Protein coding
M0QZQ3 -GENCODE BasicTSL:5
ENST00000392023.1SPTBN4-2022419678aaENSP00000375877.1
 
Protein coding
CCDS42569Q9H254-5 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000597389.5SPTBN4-2095957701aaENSP00000472136.1
 
Nonsense mediated decay
M0R1V6 -TSL:5CDS 5' incomplete
ENST00000593816.1SPTBN4-203712No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000599926.5SPTBN4-212525No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000596411.1SPTBN4-2071885No protein-
 
Retained intron
--TSL:2
ENST00000596900.5SPTBN4-2081857No protein-
 
Retained intron
--TSL:1
ENST00000593932.1SPTBN4-2041015No protein-
 
Retained intron
--TSL:1
ENST00000595690.1SPTBN4-206763No protein-
 
Retained intron
--TSL:2
ENST00000598775.1SPTBN4-211580No protein-
 
Retained intron
--TSL:3