Human (GRCh38.p14)
Description

seizure related 6 homolog [Source:HGNC Symbol;Acc:HGNC:15955]

Location

Chromosome 17: 28,954,901-29,006,440 reverse strand.

GRCh38:CM000679.2

About this gene

This gene has 9 transcripts (splice variants), 245 orthologues and 39 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000317338.17SEZ6-2014206994aaENSP00000312942.11
 
Protein coding
CCDS45639Q53EL9-1 NM_178860.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT2TSL:1
ENST00000360295.13SEZ6-2024306993aaENSP00000353440.9
 
Protein coding
CCDS45638Q53EL9-3 -GENCODE basicAPPRIS P4TSL:5
ENST00000442608.7SEZ6-2033805980aaENSP00000403784.3
 
Protein coding
A0A0A0MSU7 -GENCODE basicTSL:5
ENST00000540632.6SEZ6-2073804919aaENSP00000437650.2
 
Protein coding
H0YF95 -TSL:1CDS 5' incomplete
ENST00000535262.1SEZ6-204807101aaENSP00000440216.1
 
Protein coding
H0YFT6 -TSL:3CDS 5' incomplete
ENST00000539265.1SEZ6-205601131aaENSP00000443589.1
 
Protein coding
H0YGK0 -TSL:2CDS 5' incomplete
ENST00000585644.1SEZ6-20957556aaENSP00000466107.1
 
Protein coding
K7ELJ4 -TSL:4CDS 3' incomplete
ENST00000540419.5SEZ6-2063468454aaENSP00000440764.1
 
Nonsense mediated decay
H0YFX0 -TSL:2CDS 5' incomplete
ENST00000544224.2SEZ6-208807No protein-
 
Retained intron
--TSL:2