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Human (GRCh37.p13)
Description

contactin 1 [Source:HGNC Symbol;Acc:2171]

Gene Synonyms

F3, GP135

Location

Chromosome 12: 41,086,244-41,466,220 forward strand.

GRCh37:CM000674.1

About this gene

This gene has 12 transcripts (splice variants), 17 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000551295.2CNTN1-00155571018aaENSP00000447006.1
 
Protein coding
CCDS8737F8VQW3 F8VUI8 F8VUI9
F8VX96 Q12860
NM_001843
NP_001834
GENCODE basic
ENST00000347616.1CNTN1-20133931018aaENSP00000325660.3
 
Protein coding
CCDS8737F8VQW3 F8VUI8 F8VUI9
F8VX96 Q12860
-GENCODE basic
ENST00000348761.2CNTN1-00233281007aaENSP00000261160.3
 
Protein coding
CCDS8738Q12860 NM_175038
NP_778203
GENCODE basic
ENST00000547849.1CNTN1-0043125627aaENSP00000448653.1
 
Protein coding
CCDS58225F8VQW3 F8VUI8 F8VUI9
F8VX96 Q12860
NM_001256064
NP_001242993
GENCODE basic
ENST00000547702.1CNTN1-0033033627aaENSP00000448004.1
 
Protein coding
CCDS58225F8VQW3 F8VUI8 F8VUI9
F8VX96 Q12860
NM_001256063
NP_001242992
GENCODE basic
ENST00000360099.3CNTN1-2021963627aaENSP00000353213.3
 
Protein coding
CCDS58225F8VQW3 F8VUI8 F8VUI9
F8VX96 Q12860
-GENCODE basic
ENST00000552913.1CNTN1-00657272aaENSP00000449706.1
 
Protein coding
F8VQW3 F8VX96 -CDS 3' incomplete
ENST00000551424.1CNTN1-00555562aaENSP00000450412.1
 
Protein coding
F8VQW3 -CDS 3' incomplete
ENST00000548005.1CNTN1-00855385aaENSP00000447862.1
 
Protein coding
F8VQW3 F8VUI8 F8VX96
-CDS 3' incomplete
ENST00000552248.1CNTN1-00746390aaENSP00000447860.1
 
Protein coding
F8VQW3 F8VUI8 F8VUI9
F8VX96
-CDS 3' incomplete
ENST00000548481.1CNTN1-01051257aaENSP00000449517.1
 
Nonsense mediated decay
H0YIJ1 -CDS 5' incomplete
ENST00000550305.1CNTN1-009731No protein-
 
Processed transcript
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Gene-based displays