Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 17 exons, is annotated with 58 domains and features, is associated with 21817 variant alleles and maps to 687 oligo probes.

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

Protein domains for ENSP00000353440.9