Human (GRCh37.p13)
Description

ceroid-lipofuscinosis, neuronal 6, late infantile, variant [Source:HGNC Symbol;Acc:2077]

Gene Synonyms

CLN4A, FLJ20561, HsT18960, nclf

Location

Chromosome 15: 68,499,330-68,549,549 reverse strand.

GRCh37:CM000677.1

About this gene

This gene has 10 transcripts (splice variants), 191 orthologues and is associated with 8 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000249806.5CLN6-0012242311aaENSP00000249806.5
 
Protein coding
CCDS10227Q9NWW5 NM_017882.2Ensembl CanonicalGENCODE Basic
ENST00000538696.1CLN6-0041343343aaENSP00000445770.1
 
Protein coding
B4DDH6 -GENCODE Basic
ENST00000565471.1CLN6-0081074158aaENSP00000457384.1
 
Protein coding
H3BTY4 -GENCODE Basic
ENST00000566347.1CLN6-005981248aaENSP00000457783.1
 
Protein coding
H3BUT1 -GENCODE Basic
ENST00000418702.2CLN6-201945182aaENSP00000393826.2
 
Protein coding
E7ESV1 -GENCODE Basic
ENST00000564752.1CLN6-006900213aaENSP00000457822.1
 
Protein coding
H3BUV4 -GENCODE Basic
ENST00000567060.1CLN6-003945105aaENSP00000454818.1
 
Nonsense mediated decay
H3BNF1 --
ENST00000569336.1CLN6-009582No protein-
 
Processed transcript
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ENST00000564846.1CLN6-0021762No protein-
 
Retained intron
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ENST00000563917.1CLN6-007576No protein-
 
Retained intron
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