Human (GRCh37.p13)
Description

formin 2 [Source:HGNC Symbol;Acc:14074]

About this transcript

This transcript has 18 exons, is annotated with 33 domains and features, is associated with 176402 variant alleles and maps to 828 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000319653.9FMN2-00164341722aaENSP00000318884.9
 
Protein coding
CCDS31069B4DN09 Q96L17 Q9NZ56
NM_020066.4GENCODE basic
ENST00000543681.1FMN2-201290242aaENSP00000439136.1
 
Protein coding
Q2M1H5 -GENCODE basic
ENST00000545751.1FMN2-2021632318aaENSP00000437918.1
 
Protein coding
B4DP05 Q96L17 -GENCODE basic
ENST00000447095.1FMN2-003906228aaENSP00000409308.1
 
Protein coding
B0QZA8 -CDS 3' incomplete
ENST00000441342.1FMN2-00560299aaENSP00000388922.1
 
Protein coding
B0QZD5 -CDS 3' incomplete
ENST00000496950.1FMN2-002693No protein-
 
Processed transcript
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ENST00000463398.1FMN2-004571No protein-
 
Processed transcript
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Statistics

Exons: 18, Coding exons: 18, Transcript length: 6,434 bps, Translation length: 1,722 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NZ56

CCDS

This transcript is a member of the Human CCDS set: CCDS31069

Incomplete CDS

CDS 5' and 3' incomplete

Version

ENST00000319653.9

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000096217 (version 2)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.