Human (GRCh38.p14)
Description

fms related receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:3763]

Gene Synonyms

FLT, VEGFR1

Location
About this transcript

This transcript has 30 exons, is annotated with 99 domains and features, is associated with 83930 variant alleles and maps to 1078 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000282397.9FLT1-20171231338aaENSP00000282397.4
 
Protein coding
CCDS9330P17948-1 NM_002019.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000615840.5FLT1-2076502687aaENSP00000484039.1
 
Protein coding
CCDS73556P17948-2 -GENCODE basicTSL:1
ENST00000639477.1FLT1-2096337665aaENSP00000491097.1
 
Protein coding
A0A1W2PNW4 -GENCODE basicTSL:5
ENST00000541932.5FLT1-2042969733aaENSP00000437631.1
 
Protein coding
CCDS53860P17948-3 -GENCODE basicTSL:1
ENST00000539099.2FLT1-2021763541aaENSP00000442630.1
 
Nonsense mediated decay
CCDS53861P17948-4 -TSL:1
ENST00000540678.2FLT1-2031927No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000706527.1FLT1-2101865No protein-
 
Protein coding CDS not defined
---
ENST00000615611.4FLT1-2061476No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000543394.2FLT1-2051275No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000617835.5FLT1-208575No protein-
 
Protein coding CDS not defined
--TSL:1
Statistics

Exons: 30, Coding exons: 30, Transcript length: 7,123 bps, Translation length: 1,338 residues

MANE

This MANE Select transcript contains ENSP00000282397 and matches to NM_002019.4 and NP_002010.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P17948

CCDS

This transcript is a member of the Human CCDS set: CCDS9330

Transcript Support Level (TSL)

TSL:1

Version

ENST00000282397.9

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.

GENCODE basic gene

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